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Wolf-Hirschhorn syndrome
MONDO:0008684Wolf-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.
Also known as: 4p deletion syndrome, 4p- syndrome, Pitt syndrome, Pitt-Rogers-Danks syndrome, Wittwer syndrome, Wolf-Hirschhorn syndrome, Wolf-Hirschhorn syndrome, Isolated cases, chromosome 4p16.3 deletion syndrome
6 clinical trials for this condition and its sub-types.
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Disease
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Syndromic disease
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Human disease
(14)
Chromosomal disorder
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Developmental defect during embryogenesis
(7)
Disease of genetic or genomic mechanism
(2)
Multiple congenital anomalies/dysmorphic syndrome
(1)
Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
(1)
Autosomal anomaly
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Chromosome 4 disorder
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