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

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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Bibliographic Details
Main Authors: Eva-Cristiana Gavril, Alina Costina Luca, Alexandrina-Stefania Curpan, Roxana Popescu, Irina Resmerita, Monica Cristina Panzaru, Lacramioara Ionela Butnariu, Eusebiu Vlad Gorduza, Mihaela Gramescu, Cristina Rusu
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Children
Subjects:
Wolf–Hirschhorn Syndrome
4p deletion
craniofacial dysmorphism
growth retardation
IUGR
Online Access:https://www.mdpi.com/2227-9067/8/9/751

Internet

https://www.mdpi.com/2227-9067/8/9/751

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