Familial pontocerebellar hypoplasia type I with anterior horn cell disease.

Görgen-Pauly, U

Familial pontocerebellar hypoplasia type I with anterior horn cell disease. [electronic resource] - European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 1999 - 33-8 p. digital

Publication Type: Case Reports; Journal Article

1090-3798

10.1053/ejpn.1999.0177 doi


Abnormalities, Multiple--genetics
Atrophy--pathology
Cerebellum--abnormalities
Diagnosis, Differential
Fatal Outcome
Female
Humans
Infant, Newborn
Magnetic Resonance Imaging
Motor Neuron Disease--complications
Olivopontocerebellar Atrophies--complications
Pedigree
Pons--abnormalities
Pregnancy