16q24.1 microdeletion syndrome

Orpha code: 352629OMIM code:

Definition

A partial autosomal monosomy characterized clinically by lethal pulmonary disease that presents as severe respiratory distress and refractory pulmonary hypertension within a few hours after birth and typically results in death from respiratory failure within the first months of life. Characteristic histological features of lung tissue include paucity of alveolar wall capillaries, alveolar wall thickening, muscular hypertrophy of the pulmonary arteries, and malposition of the small pulmonary veins. Various additional congenital malformations may be associated, mostly gastrointestinal (intestinal malrotation and atresias, anular pancreas), genitourinary (dilatation of urinary tracts, duplicated uterus) and cardiovascular anomalies (hypoplastic left heart and other congenital heart defects).

Disease data
Classification

Disease

Synonyms
Del(16)(q24.1)
Del(16)(q24.1)
Monosomia 16q24.1
Monosomy 16q24.1
ORPHA code
352629
OMIM code
-
ICD10 code
Q93.5
ICD11 code
-

No additional description.

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