Pontocerebellar Hypoplasia Type 9: A New Case with a Novel Mutation and Review of Literature
{{output}}
Pontocerebellar hypoplasia type 9 (PCH-9) is a very rare autosomal recessive neurodegenerative disorder. Affected infants present early with severe developmental delay, spasticity, with the unique magnetic resonance imaging picture of thin corpus callosum, atr... ...
