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Article

Intrauterine Treatment of a Fetus with Familial Hypertrophic Cardiomyopathy Secondary to MYH7 Mutation.

Pediatric cardiology - 1 Dec 2015

Hill Meghan G, Sekhon Mehtab K, Reed Kathryn L, Anderson Caroline F, Borjon Nydia D, Tardiff Jil C, Barber Brent J

Abstract excerpt

There is no clear consensus on optimal management of fetuses affected by familial hypertrophic cardiomyopathy (HCM). Intrauterine treatment of the condition has not been attempted in any standardized fashion. We report the case of a fetus treated by maternal propranolol during the third trimester...

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Share to Adrenergic beta-Antagonists
Share to Cardiac Myosins
Share to Cardiomyopathy, Hypertrophic, Familial

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Myosin Heavy Chains

Share to Pregnancy Trimester, Third

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Source

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Identifiers

PMID: 26337809
DOI: 10.1007/s00246-015-1250-1
PMCID: PMC4655206

Genes

MYH7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-26337809-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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