The first Finnish patient with the Floating-Harbor syndrome: the follow-up of eight years

Sirpa Ala-Mello; Maarit Peippo

doi:10.1002/ajmg.a.30303

The first Finnish patient with the Floating-Harbor syndrome: the follow-up of eight years

Am J Med Genet A. 2004 Oct 15;130A(3):317-9. doi: 10.1002/ajmg.a.30303.

Authors

Sirpa Ala-Mello¹, Maarit Peippo

Affiliation

¹ Department of Clinical Genetics, Helsinki University Central Hospital, Helsinki, Finland. [email protected]

PMID: 15378536
DOI: 10.1002/ajmg.a.30303

Abstract

We report the follow-up data on the first Finnish patient with the Floating-Harbor syndrome (FHS) reported by us in 1996 at the age of 6 years (Ala-Mello and Peippo. We also discuss the diagnostic criteria of FHS, with a critical review of the literature.

Publication types

Case Reports

MeSH terms

Abnormalities, Multiple / genetics
Abnormalities, Multiple / pathology*
Adolescent
Child
Face / abnormalities
Finland
Follow-Up Studies
Growth Disorders / pathology*
Humans
In Situ Hybridization, Fluorescence
Male
Speech Disorders / pathology*
Syndrome