Jember Medical Journal

A Stillborn Baby with Tetra-amelia Syndrome in Jember: A Case Report

Daniel Alexander Suseno
Department of Obstetrics and Gynecology, dr. Soebandi Jember General Hospital, Patrang, Jember, Indonesia

Achmad Haykal Baswedan
Medical Doctor Clerkship, Faculty of Medicine, University of Jember, Sumbersari, Jember, Indonesia

Muhamad Dwi Eka Putra
Medical Doctor Clerkship, Faculty of Medicine, University of Jember, Sumbersari, Jember, Indonesia

Muhammad Haikal Supriyadi
Medical Doctor Clerkship, Faculty of Medicine, University of Jember, Sumbersari, Jember, Indonesia

Wahyuning Pangestu
Medical Doctor Clerkship, Faculty of Medicine, University of Jember, Sumbersari, Jember, Indonesia

DOI: https://doi.org/10.19184/jembermedicaljournal.v3i2.1057

Abstract

Tetra-amelia syndrome is a rare congenital disorder characterized by the absence of all four extremities. This extremity disorder occurs in 1 in 1,300 to 2,000 births. This condition is caused by genetic mutations in the WNT3 and RSPO2 genes. Specific risk factors for tetra-amelia syndrome remain unclear. This is also due to the lack of studies that discuss specific risk factors for tetra-amelia syndrome. In this case report, we discuss a stillborn baby with tetra-amelia syndrome to a mother with various pregnancy risk factors in Jember. This case report aims to examine the presence of several risk factors in the mother and their relationship with congenital disorders, especially tetra-amelia syndrome.

Keyword: congenital disorders, genetic disorders, malformations, still born, tetra-amelia syndrome

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Published
November 20 , 2024

Issue
Vol. 3 No. 2 (2024)

Section
Case Report

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