Walker-Warburg syndrome: A case report of congenital muscular dystrophy with hydrocephalus

Author:

Aref Fawzya,Shaaban Amin,Ahmed Abouelhassan,Gubari Maram,Hassan JoodORCID,Alharbi Mussaed,Alsubhi Kholod,Alsalhi Kareem,Albalawi Shama,Ali MohamadORCID,Ali Hiba,Filfilan NajlaORCID,Shmailah ElafORCID,Ahmed Attallah

Publisher

Elsevier BV

Reference6 articles.

1. Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly;Vuillaumier-Barrot;Am Hum Genet,2012

2. Walker-Warburg syndrome: a case with multiple uncommon features;Bedri;Sudanese J Paediatr,2011

3. Walker-Warburg syndrome;Vajsar;Orphanet J Rare Dis,2006

4. TMEM5-associated dystroglycanopathy presenting with CMD and mild limb-girdle muscle involvement;Astrea;Neuromuscul Disord,2016

5. Walker-Warburg syndrome: a case report of congenital muscular dystrophy with cerebro-ocular malformation, a rare syndrome in an African patient;Amiji I;J Pediatr, Perinatol Child Health,2019

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