Leri-Weill Dyschondrosteosis Syndrome: Analysis via 3DCT Scan

Leri-Weill Dyschondrosteosis Syndrome: Analysis via 3DCT Scan

<b>Background:</b> Leri-Weill dyschondrosteosis (LWD) is a pseudoautosomal form of skeletal dysplasia, characterized by abnormal craniofacial phenotype, short stature, and mesomelia of the upper and lower limbs. <b>Methods:</b> We describe two female patients with LWD. Their...

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Bibliographic Details
Main Authors: Ali Al Kaissi, Mohammad Shboul, Vladimir Kenis, Franz Grill, Rudolf Ganger, Susanne Gerit Kircher
Format: Article
Language:English
Published: MDPI AG 2019-05-01
Series:Medicines
Subjects:
Leri-Weil dyschondrosteosis
tomography
craniosynostosis
deficient ribs number
ischial dysplasia
coxa valga
<i>SHOX</i> gene
Online Access:https://www.mdpi.com/2305-6320/6/2/60

Internet

https://www.mdpi.com/2305-6320/6/2/60

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