Lowe Syndrome (Oculo-cerebro-renal Syndrome of Lowe): A Case Report fromEastern India

Journal Title: Journal of Krishna Institute of Medical Sciences University - Year 2014, Vol 3, Issue 1

Abstract

Lowe syndrome (the oculocerebrorenal syndrome ofLowe, OCRL) is a rare X-linked recessive metabolicdisorder that primarily affects eyes, kidneys and brain.It is caused by the deficiency of enzymephosphatidylinositol 4, 5-bisphosphate 5-phosphatase.The gene coding for this enzyme, OCRL1 and mutationsin it are responsible to cause Lowe Syndrome.We report a 6 years old boy from Eastern India, withLowe Syndrome. Diagnosis was suggested by typicalfeatures in the MRI of the brain along with other clinicalfeature and investigation.

Authors and Affiliations

Dipankar Das , Shoumini Chakravarty , Jaydeb Ray

Keywords

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  • EP ID EP120824
  • DOI -
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How To Cite

Dipankar Das, Shoumini Chakravarty, Jaydeb Ray (2014).  Lowe Syndrome (Oculo-cerebro-renal Syndrome of Lowe): A Case Report fromEastern India. Journal of Krishna Institute of Medical Sciences University, 3(1), 107-111. https://europub.co.uk./articles/-A-120824