Wiedemann–Rautenstrauch syndrome
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Wiedemann–Rautenstrauch (WR) syndrome (German pronunciation: [ˈviːdəman ˈʁaʊtn̩ʃtʁaʊx]), also known as neonatal progeroid syndrome,[1] is a rare autosomal recessive progeroid syndrome. There have been over 30 cases of WR.[2] WR is associated with abnormalities in bone maturation, and lipids and hormone metabolism.[3]
Quick Facts Other names, Specialty ...
Wiedemann–Rautenstrauch syndrome | |
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Other names | Neonatal progeroid syndrome |
This condition is inherited in an autosomal recessive manner. | |
Specialty | Endocrinology |
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