Vol. 12 (10) pp. 765-767 DOI: 10.21474/IJAR01/19694

GENETIC INSIGHTS INTO 3-M SYNDROME: A NEONATAL CASE REPORT

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Abstract

3-M syndrome is an uncommon autosomal recessive disorder. We present a case of a one-day-old infant with low birth weight, an enlarged head, and shortened limbs, initially suspected of skeletal dysplasia. Genetic testing confirmed the diagnosis of 3-M syndrome.

How to Cite This Article

Kanakaveetipranav and Vinaykumar S. (2024); GENETIC INSIGHTS INTO 3-M SYNDROME: A NEONATAL CASE REPORT, International Journal of Advanced Research (IJAR), 12 (10), 765-767, ISSN 2320-5407. DOI: https://doi.org/10.21474/IJAR01/19694

Corresponding Author

Dr Kanakaveeti Pranavkumar
Pediatrics
India

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