Retrospective Diagnosis of GM1 Gangliosidosis by Use of a Newborn-Screening Card

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Abstract
A deficiency of lysosomal β-d-galactosidase (βG; EC 3.2.1.23) is the primary defect in the three clinical forms (infantile, juvenile, and adult) of GM1 gangliosidosis and in Morquio B syndrome. Patients with the infantile form of GM1 gangliosidosis (type 1), who usually die before the age of 3 years, display the coarse face, hepatosplenomegaly, and skeletal dysplasia reminiscent of Hurler disease. Cases with later onset, described as the late infantile/juvenile form (type 2), display progressive psychomotor loss but less prominent dysmorphic changes. Extrapyramidal signs of protracted course are the major neurologic manifestations in the adult/chronic form (type 3) of GM1 gangliosidosis. Morquio B syndrome is expressed as generalized skeletal dysplasia with corneal clouding and normal intelligence (1).

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