Mosaic trisomy 15

Orpha code: 1706OMIM code:

Definition

Mosaic trisomy 15 is a rare chromosomal anomaly syndrome principally characterized by intrauterine growth restriction, congenital cardiac anomalies (incl. ventricular and atrial septal defects, patent ductus arteriosus) and craniofacial dysmorphism (incl. hypertelorism, downslanting palpebral fissures, wide nasal bridge). Patients also present brain (e.g. hypoplastic cerebellum, ventricular asymmetry), renal (e.g. small dysplastic kidneys), and/or genital (undescended testis, small penis, hypoplastic labia majora) anomalies. Digital and skin pigmentation abnormalities have also been reported.

Disease data
Classification

Malformation syndrome

Synonyms
Mosaic trisomy chromosome 15
Trisomy 15 mosaicism
ORPHA code
1706
OMIM code
-
ICD10 code
Q92.1
ICD11 code
-

No additional description.

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