10 Questions
What is the primary reason for short stature in individuals with Turner syndrome?
Presence of only one copy of the SHOX gene
What is the hallmark of cardiovascular abnormalities in individuals with Turner syndrome?
Bicuspid aortic valve
What is a common musculoskeletal finding in individuals with Turner syndrome?
Cubitus valgus
What is the primary purpose of karyotyping in individuals with Turner syndrome?
To confirm the diagnosis of Turner syndrome
What is a common endocrine abnormality in individuals with Turner syndrome?
Hashimoto thyroiditis
What is the approximate prevalence of Turner syndrome in the genetically female population in the US?
1:2,500
What is the most common cause of ovarian dysgenesis and primary ovarian insufficiency?
Chromosomal nondisjunction
What is the karyotype of an individual with complete sex chromosomal monosomy?
45,XO
What is the result of mitotic nondisjunction of an embryonic cell?
Sex chromosomal mosaicism
What is the fertility outcome for women with Turner syndrome who undergo IVF using donor oocytes and exogenous hormones?
Similar to the general population
Study Notes
Epidemiology
- Prevalence of Turner syndrome: approximately 1 in 2,500 genetically female individuals in the US
Etiology
- Caused by chromosomal nondisjunction during meiosis or mitosis
- Meiotic nondisjunction: complete sex chromosomal monosomy (45,XO; no Barr body)
- Mitotic nondisjunction of an embryonic cell: sex chromosomal mosaicism (45,XO/46,XX) with mild phenotypic expression
Pathophysiology
- Chromosomal nondisjunction → X chromosome monosomy/mosaicism
- Impaired ovarian development → malfunctioning streak gonads with connective tissue instead of normal germ cells
- Estrogen and progesterone deficiencies
Clinical Features
- Female phenotype
- Primary ovarian insufficiency with:
- Delayed puberty
- Primary amenorrhea
- Infertility (pregnancy possible via IVF with donor oocytes and exogenous estradiol 17β and progesterone)
- Lymphatic system abnormalities:
- Cystic hygroma
- Lymphedema of the hands and feet in neonatal period
- Musculoskeletal findings:
- Short stature (due to presence of only one copy of the SHOX gene)
- Shield chest
- Webbed neck
- Cubitus valgus
- Short fourth metacarpals/metatarsals
- Nail dysplasia
- High arched palate
- Low-set posterior hairline
- Cardiovascular abnormalities:
- Bicuspid aortic valve
- Coarctation of the aorta with brachial-femoral delay
- Aortic dissection and rupture
- Hypertension
Associated Disorders
- Gonadoblastoma (especially in patients with 45,XO/46,XY mosaicism)
- Malformations of the kidney and ureters (especially horseshoe kidney)
- Hashimoto thyroiditis
- Type 2 diabetes mellitus
Diagnostics
- Clinical presentation: hypergonadotropic hypogonadism (↓ estrogen, ↓ androgens, ↑ FSH, ↑ LH)
- Karyotyping: confirmatory test
Treatment
- Estrogen and progestogen substitution
- Growth hormone (GH) therapy
- Surgical removal of streak gonads
Learn about the prevalence, etiology, and pathophysiology of Turner syndrome, a chromosomal disorder affecting genetically female individuals. Understand the role of meiotic and mitotic nondisjunction in its development.
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