Myhre syndrome
Medical condition / From Wikipedia, the free encyclopedia
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Myhre syndrome is a rare genetic disorder inherited in an autosomal dominant fashion. It is caused by mutation in SMAD4 gene.
Quick Facts Other names, Specialty ...
Myhre syndrome | |
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Other names | Facial dysmorphism-intellectual disability-short stature-hearing loss syndrome |
Myhre syndrome is inherited in an autosomal dominant manner[1] | |
Specialty | Medical genetics |
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