Wolf–Hirschhorn syndrome: A case demonstrated by a cytogenetic study

We present a case with a 4p terminal deletion, evidenced in GTG-banded chromosome study. Phenotypic signs described in the classical Wolf–Hirschhorn syndrome were found on clinical examination of our patient.

Detalles Bibliográficos
Autores principales: Pokale, Yamini S., Jadhav, Ajinkya M., Kate, Ushang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3385166/
https://www.ncbi.nlm.nih.gov/pubmed/22754235
http://dx.doi.org/10.4103/0971-6866.96677
Descripción
Sumario:We present a case with a 4p terminal deletion, evidenced in GTG-banded chromosome study. Phenotypic signs described in the classical Wolf–Hirschhorn syndrome were found on clinical examination of our patient.

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