Hipomelanosis De Ito Orphanet
Cytogenetic analysis performed in one of the daughters in showed. A case report. Postzygotic Inactivating Mutation Of Kif13a Located At Chromosome 6p22 3 In A Patient With A Novel Mosaic Neuroectodermal Syndrome Journal Of Human Genetics La hipomelanosis de ito es un sndrome neurocutneo con un grado de despigmentacin drmica variable y. Hipomelanosis de ito orphanet . 10262019 HIPOMELANOSIS DE ITO PDF. Presentacin de un caso. El desarrollo de hipomelanosis se basa en una violacin de la produccin de melanina por los melanocitos localizados en el grosor de la piel. Other symptoms may include varying degrees of learning disability seizures increased body hair scoliosis and strabismus. Una malattia neurocutanea multisistemica con lesioni cutanee ipopigmentate lungo le linee di Blaschko. Deysi Licourt Otero 1 Prisca Saray Nez Milin 2 Estrella Labrador Rodrguez 3Yazmn Contreras Contreras 4 Ilena A. October 26 2019. 122004 La hipomelanosis de Ito HI o incontinentia pigmen