Turner syndrome (mechanism of disease)

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  • Опубліковано 20 сер 2024
  • This is a flowchart on Turner syndrome, covering the etiology, pathophysiology, manifestations, and pharmacology/interventions.
    ADDITIONAL TAGS:
    Horseshoe kidneys
    Risk factors / SDOH
    Cell / tissue damage
    Hormonal imbalance
    Turner syndrome
    Medicine / procedure
    Infectious / microbial
    Biochem / molecular bio
    Other medical conditions
    Signs / symptoms
    Tests / imaging / labs
    Embryology / development
    Genetics / hereditary
    Neurocog / psychiatry
    Pathophysiology
    + Pharmacology
    Etiology
    Manifestations
    Partially or completely missing an X chromosome
    Sporadic nondisjunction of sex chromosomes during parental gamete meiosis → complete chromosomal monosomy
    Karyotype:
    45,XO / 46,XX
    Sporadic nondisjunction of sex chromosomes during embryonic cell mitosis → sex chromosomal mosaicism
    Karyotype: 45,XO (no Barr body)
    Milder phenotype
    Impaired ovarian development
    Malfunctioning streak gonads with connective tissue replacing normal germ cells
    ↑ risk of X-linked recessive conditions
    Low hairline (prominently in posterior)
    Low-set ears
    Small lower jaw; high arched palate
    Wide, web-like neck; cystic hygroma
    Shield-shaped chest
    Aortic coarctation / dissection → rupture
    Broad chest, wide-spaced nipples
    Cubitus valgus
    Renal malformations: horseshoe kidneys, renal agenesis
    Short fingers and toes; nail dysplasia
    Pregnancy
    ↓ estrogen;
    ↓ progesterone
    Bicuspid aortic valve
    One SHOX gene (on X chromosome) → short stature
    ↑ FSH, ↑ LH
    Hashimoto thyroiditis
    Type 2 diabetes mellitus
    Osteoporosis → pathologic fractures
    Delayed puberty
    Primary amenorrhea
    Infertility (except in IVF)
    Sküskü15, CC BY-SA 4.0 creativecommon..., via Wikimedia Commons
    Estrogen and progesterone substitution
    Surgical removal of streak gonads
    Growth hormone therapy

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