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Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome

ORPHA:231720Malformation syndromeAutosomal recessiveInfancy, Neonatal

Ассоциированные гены (1)

LHX3
LIM homeobox 3
Disease-causing germline mutation(s) in
OMIM: 600577

Фенотипы (10)

Очень частый (80–99%)9
HP:0000407Sensorineural hearing impairment
HP:0000470Short neck
HP:0000824Decreased response to growth hormone stimulation test
HP:0003423Thoracolumbar kyphoscoliosis
HP:0004322Short stature
HP:0008213Gonadotropin deficiency
HP:0008245Pituitary hypothyroidism
HP:0010627Anterior pituitary hypoplasia
HP:0012287Hypothalamic luteinizing hormone-releasing hormone deficiency
Периодический (5–29%)1
HP:0011748Adrenocorticotropic hormone deficiency

Эпидемиология (2)

Cases/families
Worldwide
Point prevalence
<1 / 1 000 000
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы