This document discusses various methods for identifying sex, including:
1. Certain evidence includes presence of testes in males and ovaries in females, shown by ejaculation and menstruation after puberty.
2. Probable evidence includes sex-specific physical characteristics like breasts or facial hair.
3. Nuclear sexing examines Barr bodies, Davidson bodies, and Y chromosomes to determine sex.
4. Some intersex conditions exist where characteristics of both sexes are present, like Klinefelter's or Turner's syndromes.
5. Skeletal analysis, especially of the pelvis and skull, can determine sex with up to 100% accuracy.
AIS is a genetic condition where affected people have male chromosomes and male gonads with complete or partial feminization of the external genitals
An inherited X-linked recessive disease with a mutation in the Androgen Receptor (AR) gene resulting in:Functioning Y sex chromosome and abnormality on X chromosome
AIS is a genetic condition where affected people have male chromosomes and male gonads with complete or partial feminization of the external genitals
An inherited X-linked recessive disease with a mutation in the Androgen Receptor (AR) gene resulting in:Functioning Y sex chromosome and abnormality on X chromosome
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Klinefelter syndrome is a genetic condition affecting males, and it often isn't diagnosed until adulthood. Klinefelter syndrome may adversely affect testicular growth, resulting in smaller than normal testicles, which can lead to lower production of testosterone.
Klinefelter syndrome (KS) is a condition that occurs in males when they have an extra X chromosome. Some males with KS have no obvious signs or symptoms while others may have varying degrees of cognitive, social, behavioral, and learning difficulties. Adults with Klinefelter syndrome may also have primary hypogonadism (decreased testosterone
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2. Most certain evidences:
Presence of testis in males & ovaries in
females.
Shown by ejaculation & menstruation
respectively after puberty in males &
females.
3. Highly probable evidences:
Females: Presence of breast, vagina,
appropriate muscular development,
absence of moustache, beard, chest hair.
Males: Absence of breast tissue,
appropriate muscular development,
Presence of penis, moustache, beard,
chest hair.
5. NUCLEAR SEXING
The sex can be determined by studying the
presence of:
Barr bodies
Davidson’s bodies and
‘Y’ chromosomes.
6. Barr bodies (Sex Chromatin)
It is plano convex nuclear condensation seen at the inner
surface of the nuclear membrane.
In females more than 40% of nuclei of buccal mucosa contain
chromatin body (chromatin positive),
in males only less than 10% of nuclei contain chromatin body
(chromatin negative).
The ideal tissues to study Barr bodies are buccal mucosa,
skin, smooth muscle and cartilage.
Medico Legal Importance: To differentiate between males &
females
7. Davidson body
In females, upto 6% of polymorphic
W.B.C’s (i.e. neutrophils and eosinophils)
show a thin stalked drumstick like
projection at the periphery of the nucleus.
This is absent in males.
8. Y- Chromosomes:
The ‘Y’ Chromosomes present in males are
fluroscent for the dye Quinacrine
dihydrochloride.
Blood stains, cartilage, bone marrow, teeth
pulp and hair root pulp can be used as
specimens.
9. INTERSEX STATES
These are the conditions wherein both male and
female characters coexist in varying degrees in
the same individual.
Gonadal agenesis – gonads (either ovaries or
testes) fail to develop. The nuclear sex is
chromatin negative.
Gonadal dysgenesis – External genital organs
are present, but the testes or ovaries fail to
develop at puberty.
11. Klinefelter’s syndrome
Anatomical structure in male,
but the nuclear sexing is female (chromatin
positive).
The chromosomal pattern is 47XXY.
Usually undiagnosed till puberty.
12. Klinefelter’s syndrome
Testes are small & firm in consistency, aspermia, No
semen, Hyalinised testis (histologically).
Gynaecomastia is usual finding.
Sexual Euinacioidism
(long arm& legs, scanty public hair growth. may not have
hair growth over face)
The person is usually tall with long slender arm’s & legs,
scanty or absent facial hair, axillary hair and pubic hair, thin
voice (Sexual Euinacioidism).
13. Turner’s syndrome
Anatomical structure is female
nuclear sexing is male (chromatin
negative).
The chrosomal pattern is 45 XO.
14. Turner’s syndrome
. The person is usually of short stature. There is
lack of development of secondary sexual
characteristics associated with primary
amenorrhoea, grossly undeveloped breast with
widely spaced nipples, scanty public & axillary
hair, infantile tubes and streak ovaries (no ovarian
follicle, contains fibrous tissue). Congenital
anomalies like Web neck, cubitus valgus,
coarctation of aorta, osteoporosis, renal
abnormalities, red green colour blindness.
15. True hermaphroditism
A rare condition, where in external
genitalia may be of both sexes, but
internally there is presence of both testes
& ovaries and ovotestes.
16. Pseudohermaphroditism
External characteristics of one sex, with
gonads of opposite sex
Male pseudohermaphroditism:
Nuclear sex XY, sex organs & sexual
characteristic of female form
Female pseudohermaphroditism:
Nuclear sex XX, sex organs & sexual
characteristic of male form
17. Medico Legal Importance of sex:
Marriage, divorce, Nullity of marriage,
inheritance, rape, maternity, paternity,
employment, contesting for election & other
civil rights.
18. ACCURACY OF SEXING….KROGMAN
ENTIRE SKELETON… 100%
PELVIS & SKULL…….98%
PELVIS………………..95%
SKULL…………………90%
LONG BONES………..80%
19. MALE
BONY FRAME MASSIVE
INLET DEEP & NARROW
ILIUM LESS EXPANDED
ANTERIOR SUPERIOR
ILIAC SPINES NOT
WIDELY SEPARATED
FEMALE
LESS MASSIVE
SHALLOW & WIDE
MORE EXPANDED
WIDELY SEPARATED
PELVIS
21. MALE
ACETABULA WIDER
AND DEEPER
FEMALE
NARROWER AND SHALLOWER
MALE
LONG AND NARROW
WELL MARKED
PROMONTORY
CURVE IS EQUAL OVER
ENTIRE LENGHT
FEMALE
WIDE AND SHORT
LESS MARKED
CURVED BELOW THE CENTRE
OF 3RD
S. VERTEBRA
SACRUM
22. SKULLMALE
BIGGER ,HEAVIER, AND
MORE RUGGED.
FRONTO NASAL
ANGULATION DISTINCT
GLABELLA,SUPRAORBITAL
RIDGES MORE PRONOUNCED
ORBITAL OPENING- BIG
AND RETANGULAR
FEMALE
LIGHTER, SMALLER ,AND
LESS RUGGED.
NOT WELL MARKED
LESS PRONOUNCED
SMALL AND ROUNDED
23. MALE
LOWER JAW MORE
MASSIVE
CHIN SQUARE
SYMPHYSEAL HEIGHT MORE
RAMUS MORE BROAD
ANGLE EVERTED
FEMALE
LESS MASSIVE
POINTED OR ROUNDED
HEIGHT LESS
RAMUS LESS BROAD
NOT EVERTED
MANDIBLE