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Arthrogryposis Multiplex Congenita Associated with Lissencephaly: A Case Report
- Source :
- Neuropediatrics. 19:24-26
- Publication Year :
- 1988
- Publisher :
- Georg Thieme Verlag KG, 1988.
-
Abstract
- A child with arthrogryposis multiplex congenita and microcephaly is described. Cranial CT-scan and MRI showed abnormalities consistent with type I lissencephaly. The lissencephaly seems to be the primary cause of the congential contractures. Lissencephaly associated with arthrogryposis multiplex congenita has to be considered as a special kind of lissencephaly syndrome.
- Subjects :
- musculoskeletal diseases
congenital, hereditary, and neonatal diseases and abnormalities
Lissencephaly syndrome
Pathology
medicine.medical_specialty
Microcephaly
Chromosomes, Human, Pair 21
Lissencephaly
Type I lissencephaly
Humans
Medicine
skin and connective tissue diseases
Muscle contracture
Arthrogryposis
Arthrogryposis multiplex congenita
Electromyography
business.industry
Brain
General Medicine
medicine.disease
Tomography x ray computed
Child, Preschool
Pediatrics, Perinatology and Child Health
Female
Neurology (clinical)
Chromosome Deletion
medicine.symptom
Tomography, X-Ray Computed
business
Subjects
Details
- ISSN :
- 14391899 and 0174304X
- Volume :
- 19
- Database :
- OpenAIRE
- Journal :
- Neuropediatrics
- Accession number :
- edsair.doi.dedup.....81808457e6efbe61e791d9577729ead3