Multiple hemangiomas in a patient with a t(3q;4p) translocation: An infrequent association with Wolf–Hirschhorn syndrome

We report on the clinical phenotype of an infant with a duplication of the terminal portion of the long arm of chromosome 3(q26.3‐qter) and a deletion of the terminal portion of the short arm of chromosome 4(p16.3) with multiple hemangiomas and a hamartoma. Patients with deletions of distal 4p have...

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Veröffentlicht in:	American journal of medical genetics. Part A 2008-01, Vol.146A (2), p.219-224
Hauptverfasser:	Pardo, Sherly, Blitman, Netta, Han, Bokyung, Cohen, Ninette, Edelmann, Lisa, Hirschhorn, Kurt
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Chromosome aberrations Chromosome Deletion Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 4 Classical genetics, quantitative genetics, hybrids Complex syndromes duplication 3q syndrome Fundamental and applied biological sciences. Psychology Genetics of eukaryotes. Biological and molecular evolution hamartoma hemangioma Hemangioma - diagnosis Hemangioma - genetics Human Humans Infant Male Medical genetics Medical sciences Translocation, Genetic Trisomy Wolf-Hirschhorn Syndrome - diagnosis Wolf-Hirschhorn Syndrome - genetics Wolf–Hirschhorn syndrome
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