Extending the phenotype of lethal skeletal dysplasia type al Gazali

Am J Med Genet A. 2011 Jun;155A(6):1404-8. doi: 10.1002/ajmg.a.33990. Epub 2011 May 12.

Abstract

In this study, we describe the clinical and radiological phenotype of two patients with a rare skeletal dysplasia type al Gazali. The phenotype is characterized by brachycephaly, flat face, hypertelorism, low-set ears, hypertrichosis, hypoplastic thorax, as well as short extremities with brachydactyly. Further characteristics are severe fetal hydrops, radiologic signs of increased bone density and short, poorly modeled tubular bones with wide diaphysis and smooth, rounded metaphyses. Cortical bones as well as vertebral endplates are thick and the skull is sclerotic with prominent parietal bones and a large anterior fontanel. Our cases suggest that skeletal dysplasia type al Gazali is a lethal condition and provide further evidence that it is inherited in an autosomal recessive manner. Both morphological and radiological features of these patients are very similar, which together with the previous report may indicate the presence of a new clinical entity in the group of skeletal dysplasias with increased bone density and metaphyseal and diaphyseal involvement. Surprisingly, histological analysis of the bone tissue and the growth plate shows completely normal structure, which suggests that the skeletal dysplasia type al Gazali is a systemic disorder resulting in increased bone density and restricted growth of the skeleton.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / pathology*
  • Bone Diseases, Developmental / diagnostic imaging*
  • Collagen Type II / genetics
  • Comparative Genomic Hybridization
  • Fatal Outcome
  • Female
  • Humans
  • Infant, Newborn
  • Japan
  • Male
  • Phenotype*
  • Radiography
  • Sequence Analysis, DNA
  • Sweden
  • Syndrome

Substances

  • COL2A1 protein, human
  • Collagen Type II