Literature DB >> 645657

Dyssegmental dwarfism. A lethal anisospondylic camptomicromelic dwarfism.

J G Gruhn, R J Gorlin, L O Langer.   

Abstract

Dyssegment dwarfism is a lethal anisospondylic camptomicromelic form of growth retardation that appears to have autosomal recessive inheritance. It is characterized by short neck, cleft palate, narrow chest, severe shortening of long bones and trunk, reduced joint mobility, inguinal hernia, and probably hirsutism and hydroureter/hydronephrosis. Some cases are seen with occipital exencephalocele. The long bones are short and bent with metaphyseal flaring. The vertebral bodies are of different size and many consist of separate ossified masses. The iliac bones are small with hypoplasia of the horizontal and inferior margina. Maturation of cartilage cells at the epiphyseal plates is grossly disturbed and there are puddle-like spaces among the resting cartilage cells.

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Year:  1978        PMID: 645657     DOI: 10.1001/archpedi.1978.02120290054010

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  3 in total

1.  Dyssegmental dysplasia (report of two cases with a review of the literature).

Authors:  S Fasanelli; K Kozlowski; S Reiter; D Sillence
Journal:  Skeletal Radiol       Date:  1985       Impact factor: 2.199

2.  Congenital bowing of the long bones. A review and phenotype analysis of 13 undiagnosed cases.

Authors:  B D Hall; J Spranger
Journal:  Eur J Pediatr       Date:  1980-03       Impact factor: 3.183

3.  Dyssegmental dysplasia in siblings: prenatal ultrasonic diagnosis.

Authors:  P E Andersen; M Hauge; J Bang
Journal:  Skeletal Radiol       Date:  1988       Impact factor: 2.199

  3 in total

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