Tetra-Amelia syndrome with congenital diaphragmatic hernia - A rare entity

Authors

  • Shyam Sundar Mina
  • Sugandha Arya
  • Kaifi Siddiqui
  • Meetu Salhan
  • Deepika Mina

DOI:

https://doi.org/10.32677/IJCH.2017.v04.i03.046

Keywords:

Diaphgramatic hernia, Malformation, Pulmonary hypoplasia, Tetra-Amelia syndrome

Abstract

Tetra-Amelia syndrome is a very rare disorder characterized by the absence of all four limbs. “Tetra” is the Greek word for “four” and “Amelia” refers to the failure of an arm or leg to develop before birth. This syndrome can also cause severe malformations of other parts of the body, including the face and head, heart, nervous system, skeleton, and genitalia. Tetra-Amelia syndrome with diaphragmatic defects (pulmonary hypoplasia) in a newborn is extremely rare entity. We report a very rare case of Tetra-Amelia associated with congenital diaphragmatic hernia.

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Published

2017-09-26

Issue

Section

Case Reports

How to Cite

Tetra-Amelia syndrome with congenital diaphragmatic hernia - A rare entity. (2017). Indian Journal of Child Health, 4(3), 457-458. https://doi.org/10.32677/IJCH.2017.v04.i03.046