Sex
Klinefelter Syndrome
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Klinefelter Syndrome
Epidemiology
Most common major sexual differentiation abnormality
Incidence
of Klinefelter Syndrome in specific cohorts
Newborn males: 1 in 500 to 1000
Male
Breast Cancer
: 7.5%
Infertile males: 3%
Mild
Mental Retardation
: 1%
Pathophysiology
Results in testicular dysgenesis
Chromosomal abnormality with 47,XXY karyotype
Abnormality of nondisjunction during meiosis
Maternal or paternal origin
Most of additional X
Chromosome
is inactivated
Functioning extra genes confer
Phenotype
More severe cases with XXXY, XXXXY or XXYY
Less severe cases with mosaicism (>1 cell line)
Signs
Late Eunuchoid body proportions
Tall, slim and underweight
Long legs and short torso
Obesity
and varicosities may occur in 33% of patients
Hypergonadotropic Hypogonadism
Testes
small and firm (usually <2.0 cm or 2 ml)
Penis
small
Azoospermia or
Oligospermia
(and
Infertility
)
Other signs of
Hypoandrogenism
Gynecomastia
(bilateral and painless)
Decreased facial hair, but pubic hair abundant
Labs
Karyotype: XXY
Post-
Puberty
labs
Follicle Stimulating Hormone
(FSH) increased
Leutinizing
Hormone
(LH) increased
Inhibin B decreased
Increased
Estradiol
to
Testosterone
ratio
Associated Conditions
Mild
Mental Retardation
Motor function delay
Language comprehension problems
Speech may also be affected
Learning Disorder
s
Attention Deficit Disorder
Dyslexia
Social maladjustment
Mental illness
Thyroid
dysfunction
Diabetes Mellitus
Lung
disease
Breast Cancer
(20x risk of healthy men)
Osteoporosis
Management
Gene
ral
Complete neurodevelopment evaluation at diagnosis
Indicated if diagnosis in childhood
Breast Cancer
surveillance
Management
Testosterone Replacement
after age 11
Start
Long acting
Testosterone
25-50 mg IM q3-4 weeks
Increase
Testosterone
dose by 50 mg q6-9 months
Goal: 200 to 250 mg q3-4 weeks
Maintenance
Convert to
Testosterone
patches when at 200-250 mg
Resources
American Association for Klinefelter Syndrome
http://www.aaksis.org
Klinefelter Syndrome Support Group
http://klinefeltersyndrome.org
References
Mendoki (1991) J Am Acad Child Adolesc Psychiatry 30 [PubMed]
Schwartz (1991) Endocrinol Metab Clin North Am 20:153 [PubMed]
Smyth (1998) Arch Intern Med 158(12):1309-14 [PubMed]
Behrman (2000) Nelson Pediatrics, Saunders, p. 1746-9
Wattendorf (2005) Am Fam Physician 72:2259-62
Wilson (1991) Harrison's Medicine, McGraw-Hill, p. 1800
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