A misleading presentation of juvenile Tay Sachs disease

Rev Neurol (Paris). 2020 Mar;176(3):213-214. doi: 10.1016/j.neurol.2019.06.011. Epub 2019 Sep 19.

Authors

G Zouiri¹, H Rhouda², Y Kriouile²

Affiliations

¹ Unit of neuro-pediatric and neuro-metabolic diseases, Pediatrics 2, Children's Hospital of Rabat Morocco, University of Mohammed V Souissi Rabat, Rabat 11000 Morocco. Electronic address: dr.zouiri@gmail.com.
² Unit of neuro-pediatric and neuro-metabolic diseases, Pediatrics 2, Children's Hospital of Rabat Morocco, University of Mohammed V Souissi Rabat, Rabat 11000 Morocco.

PMID: 31543363
DOI: 10.1016/j.neurol.2019.06.011

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Child
Child, Preschool
Consanguinity
DNA Mutational Analysis
Diagnosis, Differential
Epilepsy / diagnosis
Epilepsy / genetics
Female
Hexosaminidase A / genetics
Humans
Male
Morocco
Siblings
Tay-Sachs Disease / diagnosis*
Tay-Sachs Disease / genetics

Substances

Hexosaminidase A

Supplementary concepts

Tay-Sachs Disease, Juvenile