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PLIN1-related familial partial lipodystrophy

ORPHA:280356DiseaseAutosomal dominantChildhood

Ассоциированные гены (1)

PLIN1
perilipin 1
Disease-causing germline mutation(s) in
OMIM: 170290

Фенотипы (16)

Облигатный (100%)7
HP:0000822Hypertension
HP:0000842Hyperinsulinemia
HP:0000877Insulin-resistant diabetes mellitus at puberty
HP:0000956Acanthosis nigricans
HP:0001397Hepatic steatosis
HP:0002155Hypertriglyceridemia
HP:0100578Lipoatrophy
Очень частый (80–99%)5
HP:0000789Infertility
HP:0003635Loss of subcutaneous adipose tissue in limbs
HP:0003758Reduced subcutaneous adipose tissue
HP:0008981Calf muscle hypertrophy
HP:0009017Loss of gluteal subcutaneous adipose tissue
Частый (30–79%)4
HP:0000147Polycystic ovaries
HP:0000876Oligomenorrhea
HP:0001395Hepatic fibrosis
HP:0003117Abnormality of circulating hormone level

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