Not a little of a popular notion with regard to the influence of

maternal impression is due to the repetition of certain {66} village

gossip which by no means loses its point or effectiveness passing from

mouth to mouth. On the other hand, maternal impressions have been

exploited by novelists, who have found that the morbid curiosity of

women particularly with regard to this subject may make their stories

more widely read. Lucas Malet, who, in spite of the apparently

masculine pseudonym, is really the late Rev. Charles Kingsley's

daughter, has recently called renewed attention to this subject by her

novel "Sir Richard Calmady." In this the hero is born with both his

lower limbs missing from just below the knees. The author has been

careful, however, with regard to the details of the supposed maternal

impression to which this deformity is attributed. A young married

woman in the early part of her first pregnancy has her husband, whom

she loves very dearly, brought back to her with both his limbs taken

off by a shocking accident which resulted fatally. It is not

impossible, some physicians might think, to consider that so severe a

shock could produce a very deleterious effect upon the foetus. That

the result should so exactly copy the scene which was brought under

the eyes of the young mother is, however, beyond credence.

Occasionally such stories, supposedly on medical authority, find their

way into the newspapers, usually from distant parts of the country.

Certain parts of Texas particularly seem to be a fruitful source of

such stories for newspaper correspondents when there is a dearth of

other news. Farmers in thinly settled parts of the country lose a foot

in a reaping machine or a hand in the hay-cutting machine when there

is no one near to help them but their wives, with the result that the

shock to their wives proves the occasion of a similar deformity in an

as yet unborn child. Careful investigation of such cases, however, has

invariably shown that either they were completely false or that the

details showed that whatever had happened was at most a coincidence

and never a direct causative factor in the subsequent deformity.

The greatest difficulty in the mind of the medical man, with regard to

the possibility of maternal impression being communicated in any way

to the foetus, is, as we have said, his knowledge of the anatomy of

mother and foetus. While it is {67} generally supposed that the mother

is very intimately connected with her child _in utero,_ the actual

connection is by no means so direct as might be expected from the

popular impression. It is usually considered that the mother's blood

flows in the child's veins; but this is absolutely false. The child's

blood is formed independently of the mother's blood quite as is that

of the chick in the egg. At all times the blood of the child remains

quite different in constitution to that of its mother. It contains

many more red cells than does her blood and differs in other very

easily recognisable ways. Mother and child are connected by means of

an organ known as the placenta, which is attached very closely to the

uterine wall and from which through the cord the blood of the foetus

circulates. This placenta constitutes the so-called afterbirth. The

mother's blood flows in one portion of it, that of the child in

another, and they always remain distinct and separate from each other.

The gases necessary for the child's life diffuse through the membrane

which separates the two different bloods, and the salts and soluble

proteids necessary for the child's nutrition, as well as the water

necessary for its vital processes, all pass through this membrane, but

at no time is there any direct blood connection between mother and

child. Indeed, for a large part of the formative period of the foetus

life, that is, during the first two months of its existence, the ovum

is not very closely attached to the uterus at all, but grows by means

of the vital power which it has within itself.

Nor is there any direct nervous connection between mother and child;

indeed, there are no nerves at all in the placenta, and none in the

cord through which all communications between mother and child must

pass. It seems impossible to explain, then, how maternal impressions

can so effectively pass from mother to child; and indeed, the whole

subject, when looked at in this way, is apt to be considered

legendary, and the facts adduced in support of the theory of maternal

impressions are practically sure to be thought mere coincidences. A

little knowledge here might seem to justify many things that more

complete knowledge fails to be able to find any reasons for.

{68}

There is no doubt, however, that the mother's environment during

pregnancy is in general very important for the perfect development of

the intrauterine child. Many more deformed births are reported after

times of stress and trial, as, for example, after the sieges of great

cities, notably the siege of Paris in 1871, and such scenes of

desolation as occurred during the thirty years' war in Germany. These

are, however, not direct, but indirect effects of maternal

impressions. The development of the human being _in utero_ is an

extremely complicated process. Any disturbance of it, however slight,

is sure to be followed by serious consequences. Disturbances of

nutrition, such as are consequent upon the deprivation that has to be

endured in times of war or during sieges, is of itself sufficient

seriously to disturb even the uterine life of the child. In these

cases, however, there will be no traceable connection between the form

of the maternal impression and the type of deformity that occurs. This

is, however, the essence of the old theory of the direct effect of

maternal impressions, and consequently that theory must fall to the

ground.

From all that has been said, however, it becomes very clear that as

far as possible women should be shielded from the effect of various

nervous shocks during their pregnancy, and that they owe it to

themselves and their offspring to be careful with regard to any morbid

manifestations of feeling that they may detect in themselves.

JAMES J. WALSH.

{69}

VI

HUMAN TERATA AND THE SACRAMENTS

Teratology ([Greek text], a monster) is a part of biology that treats

of deviation from a normal development in man and the lower animals.

The name was adopted in 1822 by the elder Saint-Hilaire, who then

attempted to separate the results of modern exact methods of research

from the myths and loose descriptions of monsters found in the

writings of old authors. Cicero (_De Divinatione_) derives the term

monster from the proper preternatural signification looked for in the

occurrence of these abnormal beings: "Monstra, ostenta, portenta,

prodigia appellantur, quoniam monstrant, ostendunt, portendunt et

predicunt."

At the end of the seventeenth century Malpighi and Grew discovered

that plant tissue is entirely made up of microscopic spaces enclosing

fluid; they called these spaces _cells_. Different investigators found

that animal tissue is also composed of cells; and between 1835 and

1839 Schwann and Schleiden formulated the law that every metazoic

organism is made of cells, and starts from a cell.

In 1672 de Graaf discovered the mammalian ovum, in 1675 Ludwig Ham

found spermatozoa, in 1827 von Baer recognised the human ovum, but not

until 1875 was the important fact established that fertilisation is

effected by the fusion of the male and female pronuclei. This was

demonstrated by Oscar Hertwig from observation of the ova of

starfishes.

Mammalian ova, owing to an almost complete lack of yolk, are all

small. The egg of a whale is about the size of a fern-seed, but the

yolked eggs of birds are large--that of the great auk was 7.5 inches

long. In man the ovum is from 0.18 to 0.2 mm. in diameter, scarcely

visible to the {70} naked eye, and the spermatozoon is extremely

minute. The human spermatozoon is only fifty-four thousandths of a

millimetre in length, and from forty-one to fifty-three thousandths of

a millimetre are taken up by its flagellum. The essential part is from

four to six thousandths of a millimetre in length (Dr. L. N. Boston,

_Journ, of Applied Microscopy_, vol. iv. p. 1360). A line of 18 human

spermatozoa would reach only across the head of an ordinary pin. These

spermatozoa have the power of locomotion in alkaline fluid. Henle

found they can travel one centimetre in three minutes.

The human ovum and spermatozoon are single cells, and the principal

parts of a typical cell are the cytoplasm (called also the

protoplasm), and, within this, the nucleus and centrosome. The

centrosome is efficient in the process of cell-division. A few cells

have also an outer envelope or membrane, and this part is well

developed in the ovum.

The nucleus is the centre of activity in a cell. In the resting

state it is surrounded by a membrane, and within the membrane is an

intra-nuclear network made up of chromatin and linin--the chromatin

is an important element. The meshes of this network are probably

filled with fluid.

During the stages preparatory to the mitotic, or indirect, division

of a cell into two cells (one of the methods of reproduction) the

chromatin segregates in typical cases into two groups of loops, and

each group has equal portions of the chromatin. When the chromatin

is in this shape, a loop is called a chromosome.

The chromosomes are very important. They occur in constant definite

numbers in the somatic cells of the various species of many animals

and plants, and it is probable that each species of plant and animal

has its own characteristic number of chromosomes. Wilson (_The Cell

in Development and Inheritance,_ New York, 1890) gives a list of 72

species in which the number has been determined. Man has probably 16

chromosomes in the somatic cell, and the mature male and female germ

cells in man contribute eight chromosomes each to the nucleus of the

impregnated ovum.

The chromosomes transmit the physical bases of heredity from one

generation to the next, and the heritages from the two parents are

equal except in cases of prepotency. Every cell {71} in the human body

is derived from the father and the mother equally. The fact that the

woman carries a child for months in her womb means only that she

employs a peculiar method of feeding and protecting it. After its

birth she feeds it from her breasts, before birth through its

umbilical vessels, but she originally gives only the eight chromosomes

as the father does, and the child's vital principle builds up the body

from this foundation. The popular notion that the foetus in the womb

is formed through some process of literal abstraction from the

maternal tissues is no more true than that the infant is so built up

while it is suckling; both processes are merely different methods of

feeding.

All the chromosomes from the fathers of at least 200 men could fit

simultaneously on the head of one pin, yet virtually, not merely

potentially, half the bodily substance of that multitude, and all the

physical characteristics derived from the 200 fathers, are indubitably

contained in those chromosomes and nowhere else, unless by a special

creation they are infused with the new soul, which seems to be an

altogether unreasonable alternative. This statement concerning the

minuteness of the chromosomes is not speculation--they can readily be

seen and measured with the aid of the microscope.

A human being, then, obtains eight microscopic chromosomes from his

father and eight from his mother, positively nothing more except food;

yet he develops into a man with a body made up of countless millions

of cells which expand into more than 200 bones in the skeleton and

over 200 muscles,--into the fascias, ligaments, tendons, the great and

small glands, the lymph and blood systems, the respiratory and

alimentary tracts, the skin and its appendages, and a nervous system,

which alone furnishes material for years of study if we would learn

its anatomy fully. Not only all this, but the man commonly closely

resembles his father or his mother, or some other ancestor, in

personal appearance, in certain physical tendencies, in graces or

blemishes; and furthermore, he shows inherited racial characteristics.

If a father is prepotent, he may have a greater effect in producing

the formed child than the mother has, and _vice versa,_ as when a son

closely resembles his father or his mother. {72} Prepotency, moreover,

may extend down through generations and centuries. In the streets of

Palermo to-day typical Normans may be seen, despite the intermarriages

of centuries, who are the descendants of those male Normans that went

down to Sicily with Tancred. There are Romans there, too, and

Saracens. When the Belgae--a race of tall, red-bearded men, with

elliptical skulls--went from the continent of Europe to Ireland,

probably six centuries before our era, they conquered the aborigines,

a gentle, brune race of lower stature. These Belgae became the

ancestors of the chieftain class, and their physical type persists

until to-day; so does that of the Pictish aborigines. Daniel O'Connell

had a typical Belgic body. Other big, blond Irishmen are Norse or

Danish in remote origin.

How is the extremely complex human body with its various physical

characteristics built up from the nucleus of a fecundated cell, the

ovum? The endeavour to answer this question has brought out most

ingenious speculation from nearly all the great biologists of modern

times. The question is the foundation of the theories of heredity,

and it is also fundamental in the theories of evolution.

The human ovum is a flattened spherical cell, made up of a very

delicate cell-wall, called the vitelline membrane; outside this is a

comparatively thick membrane, the zona pellucida, which is properly

not a part of the cell. Within the vitelline membrane is a granular

cytoplasm, the vitellus (yolk), and in this lies the nucleus, which

in the old text-books was called the germinal vesicle. This nucleus

contains a nucleolus.

The human spermatozoon consists of a flattened head which has a thin

protoplasmic cap extending down two-thirds of its length. In the

head is the nucleus with the chromatin. Beyond the head is the neck,

which contains the anterior and posterior centrosomes. Behind the

neck is the tail, or flagellum, in three parts,--the middle piece,

the principal part, and the end piece. From the neck to the end of

the tail centrally runs a bundle of fibrils, the axial filament. In

the middle piece these fibrils are wrapped within a single spiral

filament which winds from the neck down to the annulus at the

beginning of the principal part, and lies in a clear fluid. Without

the spiral filament, along the middle piece, is the mitochondria, a

finely granular protoplasmic layer. The principal part of the tail

consists of the axial {73} filament enclosed in an involucrum, and

the end piece is made up of this filament without the involucrum.

The head and neck of the spermatozoon, which contain the nucleus and

centrosomes, are the essential parts, and the middle piece and the

remainder of the tail appear to be used solely for locomotion and

penetration. When the head penetrates the ovum, the tail is detached

and rejected.

Our knowledge of the initial stages in the development of a human

embryo is derived indirectly from the observation of other mammals.

There are nine early human embryos reported, and the average

probable age of these is twelve days. Breuss' specimen was probably

ten days old (_Wiener med. Wochenblatt,_ 1877). Peters (_Einbettung

des mensch. Eies,_ 1899) found a smaller embryo than this. The

Breuss ovum was 5 mm. in length; Peters' was 3 by 1.5 by 1.5 mm.,

but the probable age was not given. There have been numerous embryos

more than twelve days old observed, and since the process after the

twelfth day is identical in man and the higher mammals, there is no

doubt that the first stages are also the same.

The segmentation that makes new cells is complicated, and the

outcome of the division is a ball of cells. In eggs which have a

large yolk, like those of birds, the cells form a round body resting

on the surface of the yolk, but in mammalian ova a hollow ball of

cells, or a _Morula,_ results, which lines the internal surface of

the cellular envelope. The ovum absorbs moisture by osmosis and

enlarges, and about the twelfth day after the germ-nuclei have begun

to divide, the Morula, or hollow ball of cells, called also the

_Blastodermic Vesicle,_ is formed.

The next stage in development is the establishment of two primary

germinal layers, called together the _Gastrula_, The outer layer is

the _Ectoderm_ or the _Epiblast,_ and the inner layer is the

_Endoderm_ or _Hypoblast_. In a Morula the smaller cells, which

contain less yolk-material, gradually grow around the larger

yolk-containing cells to form the Gastrula.

Between the Ectoderm and the Endoderm a layer of cells called the

_Mesoderm_ or _Mesoblast_ is next formed, and from these three layers

all the parts of the embryo are built up. From the outer Ectoderm and

the inner Endoderm those organs arise which are in the body, outer

and inner,--as the nervous system and the outer skin from the

Ectoderm, the inner entrails, the lungs and liver, from the Endoderm.

From the Mesoderm come the inner skin, the bones and muscles.

By this time the embryo is a minute longitudinal streak at the {74}

surface of one pole of the ovum. The "Primitive Trace" is like a

long inverted letter U, the legs of which are in apposition. The

Primitive Trace becomes a circular flattened disc; and it grows into

a cylindrical body by the juncture of the free margins which fold

downward and inward and meet in the median line, and this closes in

the pelvic, abdominal, thoracic, pharyngeal, and oral cavities. The

legs and arms bud from this cylinder later. While the ventral

cylinder is growing, another longitudinal cylinder is formed along

the upper surface of the embryo, which will contain the brain and

the spinal column. The subsequent development of the embryo and

foetus need not be known for an understanding of the material

considered in treating here of terata.

Human terata occur in certain rather definite, types of erroneous

development, and the classification of Hirst and Piersol (_Human

Monstrosities_, Philadelphia, 1891), which is a combination and change

of the classifications of Geoffrey Saint-Hilaire, Klebs, and Foerster,

is the most satisfactory. There are four great groups of abnormally

developed human beings: (1) Hemiteratic; (2) Heterotaxic; (3)

Hermaphroditic; (4) Monstrous.

Hemiterata are giants, dwarfs, persons showing anomalies in shape, in

colour, in closure of embryonic clefts, in absence or excess of

digits, or having other defects. This group does not come under

discussion here, but attention should be called to the fact that women

who are dwarfs are to be warned before marriage that they cannot be

delivered normally,--that the caesarean section or symphyseotomy will

be necessary, or that certain physicians will practise craniotomy in

delivering them.

The Heterotaxic group comprises persons whose left or right visceral

organs are reversed in position through abnormal embryonic

development; the liver is on the left side, the heart points to the

right, and so on.

Of the next group, the Hermaphroditic, it may be said that a true

hermaphrodite, in the full sense of the term, has not been found; but

there have been several examples of individuals who had an ovary and a

testicle, and other rudimentary sexual organs that belonged to both

male and female. Forms of apparent doubling are common, and in case of

doubt as to sex the probability leans toward the {75} masculine side.

As to marriage in such cases, questions may arise that are to be

settled by the anatomist. In dealing with double monsters it is

sometimes difficult or impossible to determine whether we have to do

with one or two individuals, and this difficulty has serious weight,

especially in the administration of baptism. It is improbable that

there is a doubling of personality in hermaphrodites. A striking

characteristic of compound terata is that the individuals are always

of the same sex; moreover, the embryonal development of reproductive

organs in general is such as almost to preclude a question of duality

of personality.

Terata, more properly so called, are divided into single, double, and

triple monsters. Single monsters may be autositic, or independent of

another embryo or foetus; or they may be omphalositic, that is,

dependent upon another embryo or foetus, which is commonly well

developed, and which supplies blood for both through the umbilical

vessels. When an omphalosite exists, the other foetus is called, in

this case also, the autosite.

The first order of autositic single monsters contains four genera with

eight species, and under these species are thirty-four varieties. They

may have imperfect limbs, no limbs, one eye in the middle of the

forehead (_cyclops_), fused lower limbs (_siren_), and so on. Some of

these monsters show a strong resemblance to lower animals, but there

is no record that is in any degree scientific of a hybrid between a

human being and a lower animal.

There are two genera of the omphalositic single monsters, with four

species. One of the twins, the autosite, is commonly a normal child;

the other, the omphalosite, may be as small as a child's fist, and be

very much deformed. Of these omphalosites the _paracephalus_ has an

imperfect head, commonly no heart, and the lungs are absent or

rudimentary. The _acephalus_ has no head, and commonly no arms; the

_asomata_ is a head more or less developed, with a sac below

containing rudiments of the trunk organs. The Acephalus is very

rare--the rarest of all monsters except the Tricephalus. There is a

fourth kind--the _foetus anideus_. This is a shapeless mass of flesh

covered with skin. There may be a {76} slight prominence with a tuft

of hair on it at one end of the mass to indicate the head. In this

monster there are more traces of bodily organs than might be expected.

These four kinds of omphalosites are either dead when born, or they

die as soon as the placental circulation is cut off. If there is any

probability of life, the physician should give them baptism before the

placental circulation is stopped.

Nothing satisfactory is known concerning the etiology of single

monsters. Landau, and other authorities as great as he is, reject

the theory that maternal impressions from fright or exposure to the

sight of hideous deformity are the cause of terata. I think the

father is accountable for terata as often as the mother is. Barnes,

an English physician, and others claim they find that terata are

frequent in consanguineous marriages, but I have not been able to

verify the assertion.

It seems a theory may be offered to explain the single terata. In

1888 Roux of Breslau by puncturing one blastomere of a frog's egg in

the two-cell stage killed the punctured blastomere without affecting

the other. The punctured blastomere remained inactive, but the other

developed into a complete _half_ embryo.

Crampton by separating and isolating the blastomeres in the two-cell

stage obtained a half embryo; and Zoja by isolating blastomeres of

the medusae, Clytia and Laodice, got _dwarfed_ larvae.

Wilson succeeded by the separation through shaking of the

blastomeres in the two-cell and four-cell stages in developing

Amphioxus larvae, which were half the natural size for the two-cell

blastomeres, and commonly half the normal size from the four-cell

blastomeres, yet in the latter some of the larvae were of the normal

size but imperfect From the eight-cell stage he got only _imperfect_.

larvae. Similar results were obtained by other operators with

various eggs.

Driesch and Morgan by removing part of the cytoplasm from a

fertilized egg of the ctenophore, Beroe, produced imperfect larvae

showing certain defects which represent the parts removed.

In these cases of injured and isolated blastomeres we have, it seems

to me, a plausible theory for the etiology of single terata. The

blastomeres in the human ovum may perhaps be injured in part by

toxins from the mother, or they may be defective through disease in

the ovum or the spermatozoon. They also may possibly be displaced

traumatically, but this seems to be doubtful.

There are three theories concerning the origin of omphalositic {77}

terata. Ahlfeld (_Missbildungen des Menschen_, Leipsic, 1882) holds

that the autosite is stronger than the omphalosite, and as a

consequence the foetal circulation in the omphalosite is reversed,

and development is thus checked. Dareste (_Production artificielle

des monstruosites_, Paris, 1876), Panum (_Beitrag zur Kenntniss der

physiol. Bedeut. der angeboren Missbildungen, Virchow's Archiv.,_

1878), Perls (_Lehrbuch der allgem. Pathologie_) and Breus (_Wiener

med. Jahrbuch_, 1882) maintain there is an inherent original defect

in the omphalositic child which prevents development of the

blood-vessels, and that Ahlfeld's theory of an indirect umbilical

connection of the omphalosite to the placenta is not probable; if it

were, omphalosites would be very common, because one of twins is

nearly always stronger than the other. Hirst and Piersol (_op. cit_)

combine these theories. This kind of monster is certainly an

imperfectly developed human individual, and even the Foetus Anideus

should receive at the least conditional baptism.

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