Osteodysplastic variant of primordial dwarfism
- 1 August 1991
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 40 (2) , 146-150
- https://doi.org/10.1002/ajmg.1320400205
Abstract
A patient with intrauterine growth retardation and marked postnatal retardation of growth had microcephaly and the orofacial and dental characteristics of the Seckel phenotype. In addition she had short forearms, metaphyseal flare, especially of the distal femora, triangular distal femoral epiphyses, and pseudoepiphyses of the hands, all characteristics of an osteodysplastic variant. Parental consanguinity suggests autosomal recessive inheritance.Keywords
This publication has 12 references indexed in Scilit:
- Osteodysplastic primordial dwarfism: Report of a further case with manifestations similar to those of types I and IIIAmerican Journal of Medical Genetics, 1989
- Seckel syndrome: an overdiagnosed syndrome.Journal of Medical Genetics, 1985
- Radiological findings in the hand in seckel syndrome (bird-headed dwarfism)Pediatric Radiology, 1983
- Studies of microcephalic primordial dwarfism I: Approach to a delineation of the seckel syndromeAmerican Journal of Medical Genetics, 1982
- Studies of microcephalic primordial dwarfism III: An intrauterine dwarf with platyspondyly and anomalies of pelvis and clavicles—osteodysplastic primordial dwarfism type IIIAmerican Journal of Medical Genetics, 1982
- Studies of microcephalic primordial dwarfism II: The osteodysplastic type II of primordial dwarfismAmerican Journal of Medical Genetics, 1982
- Familial Bird-headed Dwarfism (Seckel's Syndrome)Journal of Medical Genetics, 1973
- Bird-headed dwarfs (Seckel's syndrome)The Journal of Pediatrics, 1967
- Intrauterine growth retardationversus Silver's syndromeThe Journal of Pediatrics, 1964
- Low Birth Weight DwarfismArchives of Disease in Childhood, 1961