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Article

Floating-Harbor syndrome: description of a further patient, review of the literature, and suggestion of autosomal dominant inheritance.

European journal of pediatrics - 1 Aug 1995

Lacombe D, Patton M A, Elleau C, Battin J

Abstract excerpt

UNLABELLED: The Floating-Harbor syndrome is a growth retardation syndrome with delayed bone age, speech development, and typical facial features. The face is triangular with deep-set eyes, long eyelashes, bulbous nose, wide columella, short philtrum, and thin lips. We present an additional patient and review 16 cases from the literature. The possible phenotype in the patient's mother suggests a dominant mode of...

Topics

Age Determination by Skeleton
Child, Preschool
Chromosome Aberrations
Chromosome Disorders
Dwarfism
Facial Bones
Facies
Female
Genes, Dominant
Humans
Language Development Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Phenotype

Syndrome

Source

Identifiers

PMID: 7588969
DOI: 10.1007/BF02079072

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-7588969-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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Floating-Harbor syndrome: description of a further patient, review of the literature, and suggestion of autosomal dominant inheritance.PMID 7588969Read ↗

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Molecular Genetics and Pathogenesis of the Floating Harbor Syndrome: Case Report of Long-Term Growth Hormone Treatment and a Literature ReviewSemantic proximity Read ↗

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