Ma·ri·nes·co-Gar·land syn·drome(mah-rē-nes'kō gar'lănd), [MIM*248800]
a rare neurologic disorder characterized by cerebellar ataxia, congenital cataracts, and growth and mental retardation; autosomal recessive inheritance.
Farlex Partner Medical Dictionary © Farlex 2012
Marinesco-Sjögren syndromeAn autosomal recessive condition (OMIM:248800) characterised by congenital cataracts, cerebellar ataxia, progressive muscle weakness due to myopathy with marked muscle replacement by fat and connective tissue, and delayed psychomotor development; variably accompanied by short stature, hypergonadotrophic hypogonadism, and skeletal deformities due to muscle weakness.
Defects of SIL1, which encodes a glycoprotein required for protein translocation and folding in the endoplasmic reticulum, cause Marinesco-Sjögren syndrome.
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