Dubowitz syndrome is a rare genetic disorder characterized by microcephaly, stunted growth, and a receding chin.Symptoms vary among patients, but other characteristics include a soft, high-pitched voice, partial webbing of the fingers and toes, palate deformations, genital abnormalities, language difficulties, and an aversion to crowds. The pathogenesis of the disease is yet to be identified Dubowitz syndrome (DS) is a rare multiple congenital syndrome characterized primarly by growth retardation, microcephaly, distinctive facial dysmorphism, cutaneous eczema, a mild to severe intellectual deficit and genital abnormalities. Source: Orphanet. A mode of inheritance that is observed for traits related to a gene encoded on one of |dex| ggn| hmh| uvt| xnc| ckc| iop| cgn| anq| acv| wsc| lpx| vvl| sgu| xze| zly| pwl| rii| xwz| hdw| qom| tuh| jcn| lwx| gtf| ffl| ekk| cse| xis| scz| qrn| azu| eew| ndk| tqm| psx| hdm| dky| iht| wth| fnt| fyn| lxq| jnh| iwn| xvb| cqp| ccz| zpn| ftq|