Osteogenesis imperfecta-like syndrome with severe mental retardation and extrapyramidal tract signs

Pediatric Radiology

Volumn 28, Issue 11, 1998, Pages 856-858

  Nishimura, Gen ^a   Kurosawa, Kenzi ^b   Kobayashi, Hiroshi ^b   Kawame, Hiroshi ^b  

^a DOKKYO MEDICAL UNIVERSITY   (Japan)

^b Tokyo Metropolitan Kita Medical and Rehabilitation Center   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHILD; EXTRAPYRAMIDAL SYMPTOM; FACE MALFORMATION; FEMALE; FRACTURE; HUMAN; MENTAL DEFICIENCY; OSTEOGENESIS IMPERFECTA; OSTEOPOROSIS; PRIORITY JOURNAL;

BASAL GANGLIA DISEASES; BONE AND BONES; CHILD; DIAGNOSIS, DIFFERENTIAL; FACE; FEMALE; FRACTURES, SPONTANEOUS; HUMANS; MENTAL RETARDATION; OSTEOGENESIS IMPERFECTA; SYNDROME;

EID: 0031769647     PISSN: 03010449     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002470050482     Document Type: Article

References (5)

1. Gorlin RJ, Cohen MM, Levin LS (1990) Syndromes of the head and neck, 3rd edn. Oxford University Press, New York, pp 161-163
2. Beighton P, Winship I, Behari D (1985) The ocular form of osteogenesis imperfecta: a new autosomal recessive syndrome. Clin Genet 28: 69-75
3. Kaler SG, Garrity AM, Stem HJ, et al (1992) New autosomal recessive syndrome of sparse hair, osteopenia, and mental retardation in Mennonite sisters. Am J Med Genet 43: 983-988
4. Neimann N, Martin JJ, Vidailhet M, et al (1976) Atrophies systematisees multiples, arrieration mentale, amyotrophie neurogene et fragilite osseuse congenitale. J Neurol Sci 30: 287-297
5. Singleton EB, Merten DF (1973) An unusual syndrome of widened medullary cavities of the metacarpals and phalanges, aortic calcification and abnormal dentition. Pediatr Radiol 1: 2-7