Mendelian Rare Diseases CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P Alg11-cdg Description ALG11-CDG is a form of congenital disorders of N-linked glycosylation characterized by facial dysmorphism (microcephaly, high forehead, low posterior hairline, strabismus), hypotonia, failure to thrive, intractable seizures,[…]
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