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Speech and language delay in a patient with WDR4 mutations
Xiang Chen1, Yanyan Gao2, Lin Yang3
1Division of Neonatology, Children's Hospital of Fudan University, Shanghai 201102, PR China.
European Journal of Medical Genetics
|March 30, 2018
Summary
This study identifies two novel WDR4 gene mutations in a 6-year-old boy with primordial dwarfism (PD), expanding the known genetic causes of this rare growth disorder.
Area of Science:
- Genetics
- Human Molecular Genetics
- Pediatric Endocrinology
Background:
- Primordial dwarfism (PD) is a rare genetic disorder characterized by severe growth deficiency and distinct phenotypes.
- Several genes are implicated in PD, with WD repeat domain 4 (WDR4) recently identified as a potential cause.
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