Extending the ophthalmological phenotype of Galloway-Mowat syndrome with distinct retinal dysfunction: a report and review of ocular findings

Journal article

Open access

Peer reviewed

BMC ophthalmology, Vol.18(1), pp.147-147

22/06/2018

PMCID: PMC6013877

PMID: 29929488

Abstract

Absence of perinatal and neonatal renal dysfunction

Case Report

Galloway-Mowat syndrome

Retinal dysfunction

WDR37

url

https://doi.org/10.1186/s12886-018-0820-4View

Published (Version of record) Open

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Title: Extending the ophthalmological phenotype of Galloway-Mowat syndrome with distinct retinal dysfunction: a report and review of ocular findings
Creators - without role: Maha A. Al-Rakan - King Saud University
Manal D. Abothnain - King Saud University
Muhammad T. Alrifai - King Saud bin Abdulaziz University for Health Sciences
Majid Alfadhel - King Saud bin Abdulaziz University for Health Sciences
Publication Details: BMC ophthalmology, Vol.18(1), pp.147-147
Publisher: BioMed Central
Identifiers: 9920420408331
Academic Unit: King Saud Bin Abdulaziz University for Health Sciences; King Saud University
Language: English
Resource Type: Journal article