Myhre syndrome: the first case in Korea

Myhre syndrome (MS) is a rare autosomal-dominant disorder characterized by short stature, intellectual disability, skeletal anomalies, restricted joint mobility, distinctive facial dysmorphism, and deafness. Early diagnosis of MS is difficult because its features progress and become noticeable at sc...

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Príomhchruthaitheoirí: Dongjin Lim (Údar), Jae Hyun Kim (Údar), Jieun Lee (Údar)
Formáid: LEABHAR
Foilsithe / Cruthaithe: Korean Society of Pediatric Endocrinology, 2021-09-01T00:00:00Z.
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