Ptosis in late infantile Tay-sachs disease

Author:

Devidayal ,Marwaha R. K.,Singh Paramjit,Trehan Amita

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference17 articles.

1. Kristensson K, Sourander P, Svennerholm L. Tay-Sachs disease: A generalised metabolic disorder.Acta Paediatr Scand 1966; 55 :546–562.

2. Volk BW, Adachi M, Scheck L, Klienberg W. G5-ganglioside variant of systemic late infantile lipidosis.Arch Pathol 1969; 87:393–403.

3. Volk W, Schneck L, Adachi. Clinic, pathology and biochemistry of Tay-Sachs disease. In Vinkyn PJ and Bruyn GW, eds.Handbook of Clinical Neurology. Amsterdam, North-Holland Publishing company, 1970; 385–426.

4. Kumta NB, Irani SF, Bhide AR, Punwami DV. Hexosaminidase A deficiency (Tay-Sachs disease) : A rare inborn error of ganglioside metabolism in India. In Verma IC, ed.Medical Genetics in India. Pondicherry Auroma Enterprises, 1978; 1: 97–102.

5. Multicentric study on Genetic Counselling and Antenatal Diagnosis by ICMR Task Force on Human Genetics. 1984–87.

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1. The juvenile gangliosidoses: A timeline of clinical change;Molecular Genetics and Metabolism Reports;2020-12

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