Mosaic trisomy 14

Orpha code: 1703OMIM code:

Definition

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
Classification

Malformation syndrome

Synonyms
Mosaic trisomy chromosome 14
Trisomy 14 mosaicism
ORPHA code
1703
OMIM code
-
ICD10 code
Q92.1
ICD11 code
-

No additional description.

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