Raine dysplasia: A Brazilian case with a mild radiological involvement

Clinical Dysmorphology

Volumn 9, Issue 2, 2000, Pages 99-101

  Acosta, A X ^b   Peres, L C ^b   Chimelli, L C ^b   Pina Neto, João M ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

^b NONE

Author keywords

Autosomal recessive inheritance; Consanguinity; Osteosclerosis; Raine dysplasia; Skeletal dysplasia

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BONE DENSITY; CASE REPORT; CLINICAL FEATURE; CONSANGUINITY; FACE DYSMORPHIA; HUMAN; HUMAN TISSUE; LUNG HYPOPLASIA; MALE; NEWBORN; PREMATURITY; PRIORITY JOURNAL; RADIOGRAPHY; SKULL RADIOGRAPHY;

EID: 0034040589     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200009020-00004     Document Type: Article

References (5)

1. Kan AE, Kozlowski K (1992). New distinct lethal osteosclerotic bone dysplasia (Raine syndrome). Am J Med Genet 43:860-864.
2. Kingston HM, Freeman JS, Hall CM (1991). A new lethal sclerosing bone dysplasia. Skeletal Radiol 20:117-119.
3. Al Mane K, Coates RK, McDonald P (1996). Intracranial calcification in Raine syndrome. Pediatr Radiol 26:55-58.
4. Raine J, Winter RM, Davey A, Tucker SM (1989). Unknown syndrome: microcephaly, hypoplastic nose, exophthalmos, gum hyperplasia, cleft palate, low set ears and osteosclerosis. J Med Genet 26:786-788.
5. Rejjal A (1998). Raine Syndrome. Am J Med Genet 78: 382-385.