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Disorder of sexual development revised
Disorders Of Sexual
Development
DR.Asmaa Salah
August 2016
Sex and Gender
•Sex
• genetic sex - chromosomes
• anatomical sex - internal and
external genitalia
• sexual identity - one’s identity as
male or female
•Gender
• social meaning attached to being
male or female
• gender identity - sense of being
male or female
• gender role - expectations about
how a male or female should
behave
•Androgyny/hermaphrodism:
• sex: possessing both male and
female reproductive organs
• gender: possessing both male and
female qualities
Definition:
a congenital discrepancy between external
genitalia, gonadal and chromosomal sex .
Incidence:
Studies conducted in Western countries,
with low rates of consanguinity, show that
truly ambiguous genitalia have an
estimated incidence of 1:5,000 births.
•The incidence of ambiguous genitalia
in Saudi Arabia has been estimated at
1:2,500 live births; whilst in Egypt, it
has been estimated at 1:3,000 live
births.
Normal Prenatal Development:
Internal & External Genitalia
• Sexual differentiation:
Gonadal development Starts at 8 weeks
gestation
The sex-determining region on the Y
chromosome (SRY )dictates testicular
development and testicular hormones
promote male development
.
Disorder of sexual development revised
Pathophysiology:
A. Female infants Virilization:
They have a 46,XX karyotype, are SRY-negative,
and have exclusively ovarian tissue.
B. Inadequate virilization of male infants:
This problem is caused by inadequate
androgen production or incomplete end-
organ response to androgen.
C. Disorders of gonadal differentiation
True hermaphroditism. The presence of both a
testis and an ovary (or ovotestes) in the same
individual
D. Chromosome abnormalities, syndromes, and
associations. Gonadal dysgenesisis
ambiguous genitalia have been reported
occasionally in trisomies 13 and 18 and triploidy.
INITIAL EVALUATION
The initial evaluation of the infant with ambiguous
genitalia should include :
• History
• physical examination
• evaluation of the sex chromosomes
• assessment of internal anatomy by ultrasound
• Measurment of adrenal and gonadal steroid
secretion.
History:
Prenatal exposure to androgens (eg,
progesterones, danazol) or endocrine
disrupters ( phenytoin, aminoglutethimide).
Maternal virilization in pregnancy (placental
aromatase deficiency, luteoma).
• Family history of:
females who are childless or have amenorrhea
(androgen insensitivity).
female relatives with amenorrhea and infertility
(male pseudohermaphroditism)
unexplained infant deaths (congenital adrenal
hyperplasia).
• History of consanguinity (or homogeneous
population) (recessive disorders, eg, CAH
or disorders of androgen biosynthesis).
Physical examination:
The physical examination should include:
• General examination: should address the
presence of any of the following:
dysmorphic
• features (syndromes and chromosomal
abnormalities), hypertension or
hypotension, areolar
• hyperpigmentation, and signs of
dehydration .
2. Genitalia: careful inspection and
palpation of the genitalia
the number of urogenital openings
documented
• Measures of the phallus/clitoris and
anogenital ratio
• Bilaterally nonpalpable testes:
• ( This patient with bilateral cryptorchidism had a 46,XX
karyotype ).
•Microphallus :
(stretched penile length less than 2.5 cm
in a full-term infant); microphallus
without associated hypospadias is not
"ambiguous," but may be a marker of
other disorders.
The mean full-term length is 3.5 cm with
the 2-standard deviation range, from 2.8
to 4.2 cm.
•Clitoromegaly :
• (clitoral width >6 mm or clitoral length >9 mm) (in a 46,XX
infant with 21-hydroxylase deficiency)
• Hypospadias and unilateral
nonpalpable gonad ( mixed gonadal
dysgensis):
• Discordant genitalia and sex
chromosomes:
• (This patient with male phenotypic appearance had a 46,XX
karyotype and sex reversal)
Imaging :
1-Ultrasonography of the abdomen and pelvis:
• 2. Contrast studies to outline the internal anatomy
(sinography, urethrography,
• vesiculocystoureterography, and intravenous urography) may
be indicated before reconstructive
• surgery.
2-Retrograde urethrogram may be necessary, although most
surgeons find direct visualization by cystoscopy/vaginoscopy to
be the single best method of assessing the urethral and vaginal
anatomy.
3-In some complicated cases (particularly those infants with
elements of male and female gonads/internal reproductive
structures), laparoscopic visualization with gonadal biopsy, may
be required to completely inventory the reproductive structures
HOW TO APPROTCH:
• Karyotyping:
• The results of the karyotype permit classification of the infant
into one of three diagnostic categories that guide further
evaluation, as suggested by a consensus conference :
• XX DSD
• XY DSD
• Mixed sex chromosome DSD
Disorder of sexual development revised
Disorder of sexual development revised
• Abnormal karyotype. Mixed gonadal dysgenesis with a
dysplastic gonad is the great risk for
• infants with abnormal karyotype and ambiguous genitalia.
Hormone studies are unlikely to be
• revealing in this circumstance. DNA analysis may allow
detection of SRY gene material in 46,XX phenotypic males
• and be useful in determining whether Y material is present in
a 45,X individual, placing the patient at
• risk for gonadoblastoma.
Mangement:
1- Medication:
Medical therapy for disorders of sex development (DSDs)
depends on the underlying cause and is indicated for the
conditions associated with ambiguous genitalia, including
congenital adrenal hyperplasia (CAH).
1-Supplemental hormone therapy in cases of compromised
gonadal function .
2-Hormonal induction of puberty should attempt to replicate
normal pubertal maturation to induce secondary sexual
characteristics, a pubertal growth spurt, and optimal bone
mineral accumulation
2-Surgery:
The controversy primarily revolves around issues of gender
reassignment.
Gender assignment by the physician and family may not
correlate with gender preference by the patient in adulthood.
Remember that the most important sex organ is the brain,
which may undergo hormonal imprinting in utero.
The testes in patients with complete androgen insensitivity
syndrome and those with partial androgen insensitivity
syndrome and raised female should be removed to prevent
adult malignancy.
Preserve Fertility. In addition to addressing surgery to alter
anatomical differences, it is important to consider maintaining
potential for future fertility for those who are candidates.
Today, technological advances allow for fertility enhanced
through in vitro fertilization (IVF) and intracytoplasmic sperm
injection (ICSI).
• Advantages of Performing Early Cosmetic Genital Surgery
• it may be reasonable to advocate early surgery, between the
ages of 6 and 18 months.
normalization" of the child's atypical genitalia minimizes family
distress and mitigates stigmatization and gender-identity
confusion. Second, literature supports better surgical outcomes
when surgery is performed early (including gonadectomy).
• Advantages of Delaying Early Cosmetic Genital Surgery
• True" Sex Assignment and Gender Identity. Gender identity is
far from straightforward. It is a complex biological and
psychological process with prenatal and postnatal influences.
After gender is determined, parents are often led to believe
the true sex of their child has been identified. Parents find
comfort in knowing the "truth" (true identity) regarding their
infant's "maleness" or "femaleness" has been confirmed.
3-Psychosocial management:
provided by mental health staff with expertise in DSD should
facilitate team decisions about gender assignment/
reassignment, timing of surgery, and sex hormone
replacement.
• The following consultations may be obtained:
• Geneticist/genetic counselor
• Endocrinologist
• Surgeon
• Obstetrician/urologist
• Psychologist
Referances:
• UPTODATE
Hum Hered. 2014;77(1-4):108-17. doi: 10.1159/000360763.
Epub 2014 Jul 29.
THANKYOU

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Disorder of sexual development revised

  • 3. Sex and Gender •Sex • genetic sex - chromosomes • anatomical sex - internal and external genitalia • sexual identity - one’s identity as male or female
  • 4. •Gender • social meaning attached to being male or female • gender identity - sense of being male or female • gender role - expectations about how a male or female should behave
  • 5. •Androgyny/hermaphrodism: • sex: possessing both male and female reproductive organs • gender: possessing both male and female qualities
  • 6. Definition: a congenital discrepancy between external genitalia, gonadal and chromosomal sex .
  • 7. Incidence: Studies conducted in Western countries, with low rates of consanguinity, show that truly ambiguous genitalia have an estimated incidence of 1:5,000 births.
  • 8. •The incidence of ambiguous genitalia in Saudi Arabia has been estimated at 1:2,500 live births; whilst in Egypt, it has been estimated at 1:3,000 live births.
  • 9. Normal Prenatal Development: Internal & External Genitalia • Sexual differentiation: Gonadal development Starts at 8 weeks gestation The sex-determining region on the Y chromosome (SRY )dictates testicular development and testicular hormones promote male development
  • 10. .
  • 12. Pathophysiology: A. Female infants Virilization: They have a 46,XX karyotype, are SRY-negative, and have exclusively ovarian tissue.
  • 13. B. Inadequate virilization of male infants: This problem is caused by inadequate androgen production or incomplete end- organ response to androgen.
  • 14. C. Disorders of gonadal differentiation True hermaphroditism. The presence of both a testis and an ovary (or ovotestes) in the same individual D. Chromosome abnormalities, syndromes, and associations. Gonadal dysgenesisis ambiguous genitalia have been reported occasionally in trisomies 13 and 18 and triploidy.
  • 15. INITIAL EVALUATION The initial evaluation of the infant with ambiguous genitalia should include : • History • physical examination • evaluation of the sex chromosomes • assessment of internal anatomy by ultrasound • Measurment of adrenal and gonadal steroid secretion.
  • 16. History: Prenatal exposure to androgens (eg, progesterones, danazol) or endocrine disrupters ( phenytoin, aminoglutethimide). Maternal virilization in pregnancy (placental aromatase deficiency, luteoma).
  • 17. • Family history of: females who are childless or have amenorrhea (androgen insensitivity). female relatives with amenorrhea and infertility (male pseudohermaphroditism) unexplained infant deaths (congenital adrenal hyperplasia).
  • 18. • History of consanguinity (or homogeneous population) (recessive disorders, eg, CAH or disorders of androgen biosynthesis).
  • 19. Physical examination: The physical examination should include: • General examination: should address the presence of any of the following: dysmorphic • features (syndromes and chromosomal abnormalities), hypertension or hypotension, areolar • hyperpigmentation, and signs of dehydration .
  • 20. 2. Genitalia: careful inspection and palpation of the genitalia the number of urogenital openings documented • Measures of the phallus/clitoris and anogenital ratio
  • 21. • Bilaterally nonpalpable testes: • ( This patient with bilateral cryptorchidism had a 46,XX karyotype ).
  • 22. •Microphallus : (stretched penile length less than 2.5 cm in a full-term infant); microphallus without associated hypospadias is not "ambiguous," but may be a marker of other disorders. The mean full-term length is 3.5 cm with the 2-standard deviation range, from 2.8 to 4.2 cm.
  • 23. •Clitoromegaly : • (clitoral width >6 mm or clitoral length >9 mm) (in a 46,XX infant with 21-hydroxylase deficiency)
  • 24. • Hypospadias and unilateral nonpalpable gonad ( mixed gonadal dysgensis):
  • 25. • Discordant genitalia and sex chromosomes: • (This patient with male phenotypic appearance had a 46,XX karyotype and sex reversal)
  • 26. Imaging : 1-Ultrasonography of the abdomen and pelvis: • 2. Contrast studies to outline the internal anatomy (sinography, urethrography, • vesiculocystoureterography, and intravenous urography) may be indicated before reconstructive • surgery. 2-Retrograde urethrogram may be necessary, although most surgeons find direct visualization by cystoscopy/vaginoscopy to be the single best method of assessing the urethral and vaginal anatomy. 3-In some complicated cases (particularly those infants with elements of male and female gonads/internal reproductive structures), laparoscopic visualization with gonadal biopsy, may be required to completely inventory the reproductive structures
  • 27. HOW TO APPROTCH: • Karyotyping: • The results of the karyotype permit classification of the infant into one of three diagnostic categories that guide further evaluation, as suggested by a consensus conference : • XX DSD • XY DSD • Mixed sex chromosome DSD
  • 30. • Abnormal karyotype. Mixed gonadal dysgenesis with a dysplastic gonad is the great risk for • infants with abnormal karyotype and ambiguous genitalia. Hormone studies are unlikely to be • revealing in this circumstance. DNA analysis may allow detection of SRY gene material in 46,XX phenotypic males • and be useful in determining whether Y material is present in a 45,X individual, placing the patient at • risk for gonadoblastoma.
  • 31. Mangement: 1- Medication: Medical therapy for disorders of sex development (DSDs) depends on the underlying cause and is indicated for the conditions associated with ambiguous genitalia, including congenital adrenal hyperplasia (CAH).
  • 32. 1-Supplemental hormone therapy in cases of compromised gonadal function . 2-Hormonal induction of puberty should attempt to replicate normal pubertal maturation to induce secondary sexual characteristics, a pubertal growth spurt, and optimal bone mineral accumulation
  • 33. 2-Surgery: The controversy primarily revolves around issues of gender reassignment. Gender assignment by the physician and family may not correlate with gender preference by the patient in adulthood. Remember that the most important sex organ is the brain, which may undergo hormonal imprinting in utero.
  • 34. The testes in patients with complete androgen insensitivity syndrome and those with partial androgen insensitivity syndrome and raised female should be removed to prevent adult malignancy.
  • 35. Preserve Fertility. In addition to addressing surgery to alter anatomical differences, it is important to consider maintaining potential for future fertility for those who are candidates. Today, technological advances allow for fertility enhanced through in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI).
  • 36. • Advantages of Performing Early Cosmetic Genital Surgery • it may be reasonable to advocate early surgery, between the ages of 6 and 18 months. normalization" of the child's atypical genitalia minimizes family distress and mitigates stigmatization and gender-identity confusion. Second, literature supports better surgical outcomes when surgery is performed early (including gonadectomy).
  • 37. • Advantages of Delaying Early Cosmetic Genital Surgery • True" Sex Assignment and Gender Identity. Gender identity is far from straightforward. It is a complex biological and psychological process with prenatal and postnatal influences. After gender is determined, parents are often led to believe the true sex of their child has been identified. Parents find comfort in knowing the "truth" (true identity) regarding their infant's "maleness" or "femaleness" has been confirmed.
  • 38. 3-Psychosocial management: provided by mental health staff with expertise in DSD should facilitate team decisions about gender assignment/ reassignment, timing of surgery, and sex hormone replacement.
  • 39. • The following consultations may be obtained: • Geneticist/genetic counselor • Endocrinologist • Surgeon • Obstetrician/urologist • Psychologist
  • 40. Referances: • UPTODATE Hum Hered. 2014;77(1-4):108-17. doi: 10.1159/000360763. Epub 2014 Jul 29.

Notes de l'éditeur

  1. Development of internal sexual organs
  2. Development of external sexual organs
  3. ndividuals with 46, XX testicular disorder of sex development (46, XX testicular DSD), which is sometimes still referred to as 46, XX male syndrome, have a female karyotype, male external genitalia, two testicles, azoospermia and absence of Mullerian structures. The majority demonstrate the presence of SRY (sex-determining region of Y) within their genome, most commonly on one of the X chromosomes.
  4. Xx DSD
  5. SRY: sex-determining region on the Y chromosome; AIS: androgen insensitivity syndrome; MIS: Müllerian inhibiting substance; T: testosterone; DHT: dihydrotestosterone; LH: luteinizing hormone; p450scc: P450 side chain cleavage. * If SRY is negative in an infant with a 46XY karyotype, this indicates SRY deletion or mutation.