Short rib polydactyly syndrome type III: Histopathogenesis of the skeletal phenotype

Pediatric and Developmental Pathology

Volumn 5, Issue 1, 2002, Pages 91-96

  Corsi, Alessandro ^a   Riminucci, Mara ^a   Roggini, Mario ^b   Bianco, Paolo ^b  

^a UNIVERSITY OF L'AQUILA   (Italy)

^b SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

Endochondral bone formation; Short rib polydactyly syndromes; Skeletal dysplasias; Verma Naumoff syndrome

Indexed keywords

ARTICLE; BONE DYSPLASIA; CASE REPORT; CHONDRODYSPLASIA; DISEASE CLASSIFICATION; ENCHONDRAL OSSIFICATION; FETUS; HISTOPATHOLOGY; HUMAN; MALE; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; TISSUE DIFFERENTIATION;

ADULT; BONE DEVELOPMENT; FEMALE; HUMANS; MALE; PHENOTYPE; PREGNANCY; RIBS; SHORT RIB-POLYDACTYLY SYNDROME;

EID: 0036209902     PISSN: 10935266     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10024-001-0122-2     Document Type: Article

References (15)

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5. Lethal short rib-polydactyly syndromes: Further evidence for their overlapping in a continuous spectrum
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7. Short rib polydactyly syndrome: A single or heterogeneous entity? A re-evaluation prompted by four cases
8. Short rib polydactyly syndrome type Verma-Naumoff-Le Marec in a fetus with histological hallmarks of type Saldino-Noonan but lacking internal organ abnormalities
9. Jeune asphyxiating thoracic dystrophy and short-rib polydactyly type III (Verma-Naumoff) are variants of the same disorder
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11. Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis
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14. Histopathologic examination in osteochondrodysplasia. Time for standardization
15. Familial occurrence of a short rib syndrome with hydrops fetalis but without polydactyly