Thanatophoric skeletal dysplasia: a rare case report

Authors

  • Rishabh Arora Department of Radiodiagnosis, Srinivas Institute of Medical Science and Research Centre, Mukka, Mangalore, Karnataka, India
  • Vijaya Narayana K. Holla Department of Radiodiagnosis, Srinivas Institute of Medical Science and Research Centre, Mukka, Mangalore, Karnataka, India

DOI:

https://doi.org/10.18203/2320-6012.ijrms20241972

Keywords:

Thanatophoric dysplasia, Congenital, Curved long bones

Abstract

A diverse range of bone growth disorders known as skeletal dysplasias are brought on by new mutations in the FGFR3 gene, which cause abnormalities in the size and shape of the skeleton. We present a case of thanatophoric dysplasia diagnosed antenatally on ultrasound. G2P1L0, a 30-year-old woman, came to our radiodiagnosis department for her first pregnant ultrasound examination. The results showed a single live intrauterine baby with a head that was considerably bigger than the rest of the body, a hypoplastic nasal bone, an exceedingly thin fetal thorax, thicker soft tissue in the hands and feet, as well as bent long bones that resemble telephone receiver handles, along with bilateral club feet and trident hands.

 

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References

Sahu S, Kaur P. Thanatophoric Dysplasia: Antenatal Diagnosis. Med J Armed Forces India. 2009;65(1):87-8.

Handa A, Nishimura G, Zhan MX, Bennett DL, El-Khoury GY. A primer on skeletal dysplasias. Jpn J Radiol. 2022;40(3):245-61.

Handa A, Grigelioniene G, Nishimura G. Skeletal Dysplasia Families: A stepwise Approach to Diagnosis. Radiographics. 2023;43(5):e220067.

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Published

2024-07-18

How to Cite

Arora, R., & Holla, V. N. K. (2024). Thanatophoric skeletal dysplasia: a rare case report. International Journal of Research in Medical Sciences, 12(8), 3027–3029. https://doi.org/10.18203/2320-6012.ijrms20241972

Issue

Section

Case Reports