Evidence map›Paper›PMID 40231191›Full record

ArticleAJOG global reports2025

An attractive alternative to prenatal diagnosis: a case report of preimplantation genetic testing in familial cardiomyopathy.

Shubhra Pandey, Parth Khandhedia

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In one paragraph

Article in AJOG global reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Shubhra PandeyNova IVF Fertility Center, Surat, India (Pandey).
Parth KhandhediaCollege of Physicians and Surgeons of Mumbai, Mumbai, India (Khandhedia).

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Familial hypertrophic cardiomyopathy is an autosomal dominant familial inherited heart disease caused by mutations in the sarcomere protein that affects nearly 1 in 500 people. Genetic testing is of immense importance for familial inherited diseases. This study aimed to determine a way to allow couples with either partner or both partners with familial disease to achieve a healthy biological child. Preimplantation genetic testing for monogenic disorders of the embryos is a new technique that identifies the causative mutation in the genome of family members. The embryo trophectoderm is biopsied at the blastocyst stage of development. Subsequently, embryos are made via in vitro fertilization, and 6 to 8 cells are biopsied from the trophectoderm of the day 5 blastocyst. A couple in their early 20s consulted the hospital for preconceptional counseling for a second child. Their first child was a girl who had a heterozygous variant of chr7:128844078C>T; (HET); c.3004C>T; p.Arg1002Trp on Exon 20 with a gene transcript of filamin C (+) ENST00000 325888.13. Preconceptional pretest genetic counseling of the couple regarding the genetic aspects of the severity of the mutation and its inheritance was conducted. A heterozygous missense variation was present in the asymptomatic father, whereas the mother was normal. Posttest genetic counseling was conducted using a multidisciplinary approach, and the parents were informed about the clinical implications and the possibility of risk of transmission. Preimplantation genetic testing for monogenic disorders was performed, and 6 of 10 embryos were abnormal. A frozen-thawed embryo transfer was performed that resulted in a singleton pregnancy and the term delivery of a healthy male child. Genetic testing of embryos assists clinicians in managing couples at risk of transmission of serious genetic disorders. For couples with familial disease in either partner, medically assisted reproduction with preimplantation genetic testing for monogenic disorders is a promising strategy to achieve a healthy biological child.

Indexed as

familial disordersfamilial hypertrophic cardiomyopathyhealthy childpreimplantation genetic testingpreimplantation genetic testing for monogenic disorders

Identifiers

PMID40231191
PMCPMC11994401

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