Article
New syndromic entity of situs inversus totalis.
Clinical dysmorphology - 1 Jan 1999
Mubashir M A, Sabry M A, Farah S, Haseeb N, Quasrawi B, al-Busairi W, al-Dabbous R, al-Awadi S A, Farag T I
Abstract excerpt
A 22-year-old Bedouin female with MCA/MR has been recently ascertained. She showed profound mental retardation, proportionate short stature, facial dysmorphism, spastic quadreparesis, bilateral taliper equinovarus, brachydactyly, situs inversus totalis, and MRI findings of cerebellar/midbrain migration defects. The described phenotype represents a new syndromic situs inversus with a characteristic...
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