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Reading: Lowe syndrome: Case report of a patient with a novel mutation in the OCRL gene

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Case Reports

Lowe syndrome: Case report of a patient with a novel mutation in the OCRL gene

Authors:

Grace Angeline Malarnangai Kularatnam ,

District General Hospital Matara, Sri Lanka, LK
About Grace
District General Hospital Matara, Sri Lanka
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Vindya Subasinghe,

District General Hospital Negombo, Sri Lanka, LK
About Vindya
District General Hospital Negombo, Sri Lanka
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Dilanthi Hewa Warawitage,

Lady Ridgeway Hospital Colombo, Sri Lanka, LK
About Dilanthi
Lady Ridgeway Hospital Colombo, Sri Lanka
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Kandana Liyanage Subhashinie Jayasena,

Lady Ridgeway Hospital Colombo, Sri Lanka, LK
About Kandana
Lady Ridgeway Hospital Colombo, Sri Lanka
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Florian Recker,

University of Bonn, Bonn, Germany, DE
About Florian
University of Bonn, Bonn, Germany
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Eresha Anandanie Jasinge,

Lady Ridgeway Hospital Colombo, Sri Lanka, LK
About Eresha
Lady Ridgeway Hospital Colombo, Sri Lanka
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Samantha Waidyanatha,

Lady Ridgeway Hospital Colombo, Sri Lanka, LK
About Samantha
Lady Ridgeway Hospital Colombo, Sri Lanka
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Michael Ludwig

University of Bonn, Bonn, Germany, DE
About Michael
University of Bonn, Bonn, Germany
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Abstract

Sri Lanka Journal of Child Health, 2017; 46(3): 280-282

How to Cite: Kularatnam, G.A.M. et al., (2017). Lowe syndrome: Case report of a patient with a novel mutation in the OCRL gene. Sri Lanka Journal of Child Health. 46(3), pp.281–283. DOI: http://doi.org/10.4038/sljch.v46i3.8334
Published on 05 Sep 2017.
Peer Reviewed

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