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Albinism and Developmental Delay: The Need to Test for 15q11–q13 deletion

We report a 17-month-old African female with cutaneous and ophthalmologic features of oculocutaneous albinism type 2 as well as microcephaly, absent speech, tremulous movements. P gene mutations within the Angelman/Prader-Willi syndrome critical region at 15q11–q13 cause oculocutaneous albinism type...

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Detalles Bibliográficos
Autores principales: Saadeh, Reem, Lisi, Emily C., Batista, Denise A.S., McIntosh, Iain, Hoover-Fong, Julie E.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2007
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2128718/
https://ncbi.nlm.nih.gov/pubmed/17903679
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.pediatrneurol.2007.06.024
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