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Isolated congenital absence of bilateral femur: A rare case report with antenatal diagnosis and postnatal follow-up

We report a rare case of isolated congenital absence of the bilateral femur diagnosed antenatally in an 18-19 weeks fetus on a level II scan. The bilateral femur bones were not visualized with normal bilateral tibia and fibula. The fetus was followed with a routine growth scan at 32-33 weeks along w...

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Detalles Bibliográficos
Autores principales: Kapoor, Aakriti, Kapoor, Tushar, Kapoor, Aakaar, Kapoor, Apurva, Kapoor, Ravi, Arora, Veronica, Mehar, Deepak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168404/
https://www.ncbi.nlm.nih.gov/pubmed/35673593
http://dx.doi.org/10.25259/JCIS_219_2021
Descripción
Sumario:We report a rare case of isolated congenital absence of the bilateral femur diagnosed antenatally in an 18-19 weeks fetus on a level II scan. The bilateral femur bones were not visualized with normal bilateral tibia and fibula. The fetus was followed with a routine growth scan at 32-33 weeks along with a fetal MRI, which showed similar findings. The antenatal findings were confirmed clinically as well as with a postnatal follow-up X-Ray (infantogram) of the baby. Trio whole-exome sequencing was performed for the child as well as both the parents, which did not reveal any clinically significant variant that could explain the patient’s phenotype.