Woods black norbury syndrome: Difference between revisions

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{{SK}} Immunoneurologic disorder,X-linked
{{SK}} Immunoneurologic disorder,X-linked


Poor bladder function, Low birth weight in males. Severe neonatal hypotonia in males, Complex hereditary spastic paraplegia in females, Brisk reflexes,
==Overview==
Woods black norbury syndrome is X-linked dominant disease with IgG2 deficiency characterised by poor bladder function, low birth weight in males, severe neonatal hypotonia in males, complex hereditary spastic paraplegia in females, static reduced night vision and slowly progressive proximal muscle weakness.
 
==Pathophysiology==
==Pathophysiology==
Woods black norbury syndrome is X-linked dominant, IgG2 deficiency, Slowly progressive proximal muscle weakness, Neonatal death in males, Static reduced night vision
Woods black norbury syndrome is X-linked dominant disease.
 
==Diagnosis==
===Symptoms===
Woods black norbury syndrome is characterised by poor bladder function, low birth weight in males, severe neonatal hypotonia in males, complex hereditary spastic paraplegia in females, brisk reflexes static reduced night vision and slowly progressive proximal muscle weakness.
===Laboratory findings===
Woods black norbury syndrome is characterised by IgG2 deficiency.

Revision as of 15:35, 22 December 2015

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Jyostna Chouturi, M.B.B.S [2]

Synonyms and keywords: Immunoneurologic disorder,X-linked

Overview

Woods black norbury syndrome is X-linked dominant disease with IgG2 deficiency characterised by poor bladder function, low birth weight in males, severe neonatal hypotonia in males, complex hereditary spastic paraplegia in females, static reduced night vision and slowly progressive proximal muscle weakness.

Pathophysiology

Woods black norbury syndrome is X-linked dominant disease.

Diagnosis

Symptoms

Woods black norbury syndrome is characterised by poor bladder function, low birth weight in males, severe neonatal hypotonia in males, complex hereditary spastic paraplegia in females, brisk reflexes static reduced night vision and slowly progressive proximal muscle weakness.

Laboratory findings

Woods black norbury syndrome is characterised by IgG2 deficiency.