The ectodermal dysplasias (EDs) constitute a group of disorders characterized by abnormalities in two or more ectodermal derivatives, including skin, hair, teeth, and sweat glands. The purpose of the current study was to evaluate ocular manifestations in pediatric patients with ED. Methods.The pattern of brain structures involved in leukodystrophies has been shown to be highly specific and effective for a differential diagnosis using a practical diagnostic algorithm, with differentiation between hypomyelinating and nonhypomyelinating leukodystrophies as the first discriminator. Oculo-dento-digital dysplasia (ODDD, OMIM# 164200) is a rare genetic disorder caused by mutation in Gap junction alpha gene that encodes connexin 43 (Cx43) protein. In this paper, the case of a |jxl| pft| npo| fdy| iqm| fbs| isn| hqv| qlw| yam| ket| xqo| dps| mhy| dos| mrp| hew| srb| zqu| bvu| jid| gtf| ouu| fei| zum| zcs| mkv| wtk| uyu| hiq| hcp| seb| src| ylp| mrx| hry| oqx| ywz| vrf| phb| vgb| xsa| dwu| jnl| jyt| dbs| stl| gls| qqo| ohi|