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MAST SYNDROME

Known as: SPASTIC PARAPLEGIA 21, AUTOSOMAL RECESSIVE, SPG21 
National Institutes of Health

Related topics

Related topics

7 relations
Abnormal pyramidal signsAutosomal recessive inheritanceLower limb muscle weaknessSPG21 gene

Broader (2)

DementiaSpastic Paraplegia, Hereditary

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Exome sequencing reveals a novel homozygous mutation in ACP33 gene in the first Italian family with SPG21
SPG21, also known as Mast Syndrome (MIM 248900), is an ultra-rare autosomal recessive complicated form of hereditary spastic… 
Review
2010
Review
2010
Studies on hereditary spastic paraplegia proteins
The hereditary spastic paraplegias (HSPs) are a clinically and genetically diverse group of inherited neurological disorders that… 
1992
1992
Probable cases of mast syndrome in a non-Amish family.
gramme. This is in keeping with the tremor of other body parts, for example the wingbeating arm tremor of Wilson's disease and… 
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