Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review

Wolf–Hirschhorn syndrome (WHS), a rare disorder determined by distal 4p deletion, is characterized by a pre and postnatal growth retardation, hypotonia, intellectual disability, epilepsy, craniofacial dysmorphism, and congenital fusion anomalies. The clinical aspects are dependent on the deletion’ s...

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Detalles Bibliográficos
Autores principales: Gavril, Eva-Cristiana, Luca, Alina Costina, Curpan, Alexandrina-Stefania, Popescu, Roxana, Resmerita, Irina, Panzaru, Monica Cristina, Butnariu, Lacramioara Ionela, Gorduza, Eusebiu Vlad, Gramescu, Mihaela, Rusu, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8471045/
https://www.ncbi.nlm.nih.gov/pubmed/34572183
http://dx.doi.org/10.3390/children8090751

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8471045/
https://www.ncbi.nlm.nih.gov/pubmed/34572183
http://dx.doi.org/10.3390/children8090751

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