← Назад

Congenital analbuminemia

ORPHA:86816DiseaseAutosomal recessiveAntenatal, Infancy, Neonatal

Ассоциированные гены (1)

ALB
albumin
Disease-causing germline mutation(s) in
OMIM: 103600

Фенотипы (19)

Очень частый (80–99%)2
HP:0000969Edema
HP:0003073Hypoalbuminemia
Частый (30–79%)10
HP:0001518Small for gestational age
HP:0001622Premature birth
HP:0003075Hypoproteinemia
HP:0003077Hyperlipidemia
HP:0003124Hypercholesterolemia
HP:0005413Increased alpha-globulin
HP:0009125Lipodystrophy
HP:0010702Increased circulating antibody level
HP:0010741Pedal edema
HP:0012378Fatigue
Периодический (5–29%)7
HP:0000282Facial edema
HP:0001513Obesity
HP:0001562Oligohydramnios
HP:0002783Recurrent lower respiratory tract infections
HP:0005268Spontaneous abortion
HP:0011342Mild global developmental delay
HP:0030851Low pulse pressure

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