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Wolf-Hirschhorn syndrome
rareWolf-Hirschhorn syndrome (WHS) is a developmental disorder characterized by typical craniofacial features, prenatal and postnatal growth impairment, intellectual disability, severe delayed psychomotor development, seizures, and hypotonia.
- Identifiers
- MONDO:0008684 OMIM:194190Orphanet:280
- Part of
- Chromosome 4 short arm deletionMultiple congenital anomalies/dysmorphic syndrome-intellectual disabilitySyndromic disease
- Also known as
- 4p deletion syndrome · 4p syndrome · 4p- syndrome · chromosome 4p syndrome · chromosome 4p16.3 deletion syndrome
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