Grebe Syndrome - Case Report With Review of Literature

Authors

  • Rashmi Nagaraj Department of Paediatrics, JSS Medical College, JSSAHER, Mysore, India
  • HS Kiran Department of Internal medicine, JSS Medical College, JSSAHER, Mysore, India

DOI:

https://doi.org/10.3126/jnps.v41i3.31170

Keywords:

Acromesomelic shortening, Chondrodysplasia, Grebe syndrome, Short limb dwarfism

Abstract

Grebe syndrome is a rare genetic condition characterized by short limb dwarfism. It is transmitted by autosomal mode of inheritance. There are no associated anomalies and the affected child has normal intelligence and normal life span. This syndrome has a very low incidence and needs to be differentiated from other forms of short limb dwarfism since treatment options may vary. We have described here a severely affected case of the same with review of literature.

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Published

2021-12-31

How to Cite

Nagaraj, R., & Kiran, H. (2021). Grebe Syndrome - Case Report With Review of Literature. Journal of Nepal Paediatric Society, 41(3), 447–450. https://doi.org/10.3126/jnps.v41i3.31170

Issue

Vol. 41 No. 3 (2021)

Section

Case Reports

License

Copyright (c) 2021 Rashmi Nagaraj, HS Kiran

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