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Congenital alveolar capillary dysplasia

ORPHA:210122DiseaseAutosomal dominantInfancy, Neonatal

Ассоциированные гены (1)

FOXF1
forkhead box F1
Disease-causing germline mutation(s) in
OMIM: 601089

Фенотипы (23)

Очень частый (80–99%)2
HP:0002092Pulmonary arterial hypertension
HP:0002098Respiratory distress
Частый (30–79%)3
HP:0001643Patent ductus arteriosus
HP:0002566Intestinal malrotation
HP:0004383Hypoplastic left heart
Периодический (5–29%)18
HP:0000126Hydronephrosis
HP:0001195Single umbilical artery
HP:0001629Ventricular septal defect
HP:0001631Atrial septal defect
HP:0001636Tetralogy of Fallot
HP:0001647Bicuspid aortic valve
HP:0001650Aortic valve stenosis
HP:0001734Annular pancreas
HP:0001746Asplenia
HP:0002023Anal atresia
HP:0002251Aganglionic megacolon
HP:0002575Tracheoesophageal fistula
HP:0002580Volvulus
HP:0003468Abnormal vertebral morphology
HP:0006695Atrioventricular canal defect
HP:0010882Pulmonary valve atresia
HP:0011467Absent gallbladder
HP:0100867Duodenal stenosis

Эпидемиология (3)

Prevalence at birth
1-9 / 100 000
Canada
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