Mosaic trisomy 14

Orpha code: 1703OMIM code:

Definicja

Mosaic trisomy 14 is a rare chromosomal anomaly disorder, with a highly variable phenotype, principally characterized by growth and developmental delay, intellectual disability, body asymmetry/hypotonia, congenital heart defects, genitourinary abnormalities (cryptorchidism, micropenis, large clitoris, labial swelling), and abnormal skin hyperpigmentation. Patients usually present with craniofacial dysmorphism such as microcephaly, abnormal palpebral fissure, hypertelorism, ear abnormalities, broad nose, low-set ears, micro/retro-gnathia, and cleft or highly arched palate.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
Mosaic trisomy chromosome 14
Trisomy 14 mosaicism
Kod ORPHA
1703
Kod OMIM
-
Kod ICD10
Q92.1
Kod ICD11
-

No additional description.

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