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Wolf–Hirschhorn syndrome
Chromosomal deletion syndrome / From Wikipedia, the free encyclopedia
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Wolf–Hirschhorn syndrome (WHS) is a chromosomal deletion syndrome resulting from a partial deletion on the short arm of chromosome 4 [del(4)(p16.3)].[3] Features include a distinct craniofacial phenotype and intellectual disability.
Quick Facts Other names, Specialty ...
Wolf–Hirschhorn syndrome | |
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Other names | Chromosome deletion Dillan 4p syndrome, Pitt–Rogers–Danks syndrome (PRDS), Pitt syndrome[1][2] |
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Young girl displaying characteristic facial features of Wolf–Hirschhorn syndrome | |
Specialty | Medical genetics ![]() |
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