Familial pontocerebellar hypoplasia type I with anterior horn cell disease. [electronic resource]
Producer: 20000421Description: 33-8 p. digitalISSN:- 1090-3798
- 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
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Publication Type: Case Reports; Journal Article
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