vitalwiki

Лінійна гіпопігментація та черепно-лицьова асиметрія з акральними, очними та мозковими аномаліями

ORPHA:589608· ICD-10 Q82.4· Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies

Визначення(English summary)

A rare ectodermal dysplasia syndrome characterized by linear hypopigmentation and hypotrichosis following the lines of Blaschko, symmetric or asymmetric facial dysmorphism, and body asymmetry, in association with ocular, dental, and acral anomalies. Reported manifestations include microphthalmia, strabismus, myopia, oligodontia, microdontia, conical teeth, abnormal enamel, brachydactyly, syndactyly, and broad first toe, as well as dysmorphic facial features such as downslanting palpebral fissures, broad nasal bridge, malar hypoplasia, and microstomia. Brain imaging may show cystic leukoencephalopathy and ventricular dilation.

Поширеність
<1 / 1 000 000
Успадкування
Not applicable
Вік початку
No data available