Further delineation of spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type, with emphasis on diagnostic features
Autor: | John P. Lubicky, Charles I. Scott, Patricia Borns, Becky L.M. Carpenter, Edward A. Millar, Daniel V. Schidlow, Cheryl S. Reid, Leonard O. Langer, Barbara J. Wolfson |
---|---|
Rok vydání: | 1993 |
Předmět: |
Spondyloepiphyseal dysplasia
Male medicine.medical_specialty Limb Deformities Congenital Dwarfism Osteochondrodysplasias Calcinosis medicine Humans Abnormalities Multiple Genetics (clinical) business.industry Skull Infant Newborn Infant Extremities Syndrome medicine.disease Osteochondrodysplasia medicine.anatomical_structure Dysplasia Atlantoaxial instability Child Preschool Female Radiology business Tomography X-Ray Computed Calcification |
Zdroj: | American journal of medical genetics. 45(4) |
ISSN: | 0148-7299 |
Popis: | Further delineation of a generalized bone dysplasia which we call spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type is presented. This dwarfing condition has several serious complications, with the most common cause of death being spinal cord damage secondary to atlantoaxial instability. It is a heritable condition with an autosomal recessive mode of transmission. Radiologic diagnostic criteria are developed on the basis of studies in 8 patients with the oldest being between 4 and 5 years old. The condition is clinically and radiographically apparent neonatally or in early infancy, and it is probable that all or almost all affected individuals will come to medical attention in the age range screened by this study. |
Databáze: | OpenAIRE |
Externí odkaz: |