Neonatal Death Dwarfism in a Girl with Distinctive Bone Dysplasia Compatible with Grebe Chondrodysplasia: Analysis by CT Scan-based Phenotype

Author:

Al Kaissi Ali12,Chehida Farid Ben3,Ganger Rudolf2,Grill Franz2

Affiliation:

1. Department of First Medical, Ludwig Boltzmann Institute of Osteology, Hanusch Hospital of WGKK and AUVA Trauma Centre Meidling, Hanusch Hospital, Vienna, Austria

2. Department of Paediatric, Orthopaedic Hospital of Speising, Vienna, Austria

3. Department of Imaging, Center of Radiology, Studies-Ibn Zohr Institute, Tunis, Khadra, Tunisia

Abstract

We report on a female fetus noted to have severe malformative type of skeletal dysplasia on ultrasonography done at 35 weeks gestation. The girl died shortly after birth. Clinical examination showed a fetus with severe dwarfism, extensive long and short bones, and bone deficiencies associated with multiple dislocations. Computed tomography (CT) scan-based phenotype showed a complex constellation of malformations consistent with the diagnosis of Grebe syndrome. Parents being first cousins (consanguineous marriage) strongly suggests autosomal recessive pattern of inheritance. To our knowledge, this is the first report of neonatal death dwarfism of Grebe syndrome analyzed by CT scan-based phenotype.

Publisher

Scientific Scholar

Subject

Radiology Nuclear Medicine and imaging

Reference10 articles.

1. Neonatal death dwarfism. (A further report);Kozlowski;Rofo,1978

2. Le nanisme acromesomelique;Maroteaux;Presse Med,1971

3. Die Achondrogenesis. ein einfach rezessives Erbmerkmal;Grebe;Folia Hered Path,1952

4. Grebe syndrome: Clinical and radiographic findings in affected individuals and heterozygous carriers;Costa;Am J Med Genet,1988

5. Du Pan syndrome phenotype caused by heterozygous pathogenic mutations in CDMP1 gene;Szczaluba;Am J Med Genet A,2005

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