31Oct 2024

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

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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.


[Kanakaveetipranav and Vinaykumar S. (2024); GENETIC INSIGHTS INTO 3-M SYNDROME: A NEONATAL CASE REPORT Int. J. of Adv. Res. (Oct). 765-767] (ISSN 2320-5407). www.journalijar.com


Dr Kanakaveeti Pranavkumar
Pediatrics
India

DOI:


Article DOI: 10.21474/IJAR01/19694      
DOI URL: https://dx.doi.org/10.21474/IJAR01/19694