http://www.cnr.it/ontology/cnr/individuo/prodotto/ID21227
Inverted duplication of 15q with terminal deletion in a multiple malformed newborn with intrauterine growth failure and lethal phenotype. (Articolo in rivista)
- Type
- Label
- Inverted duplication of 15q with terminal deletion in a multiple malformed newborn with intrauterine growth failure and lethal phenotype. (Articolo in rivista) (literal)
- Anno
- 2004-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/ajmg.a.30112 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Genesio R; De Brasi D; Conti A; Borghese A; Di Micco P; Di Costanzo P; Paladini D; Ungaro P; Nitsch L. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#altreInformazioni
- La scheda presente del database ISI Web of science presenta un codice ISSN erroneo. (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.30112/abstract;jsessionid=A4C329AC95679524928F59A7020A598E.d03t02 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Dipartimento di Biologia e Patologia Cellulare e Molecolare, Universita` Federico II, Napoli, Italy
BioGeM Consortium, Universita` Federico II, Napoli, Italy
Dipartimento di Pediatria, Universita` Federico II, Napoli, Italy
Dipartimento di Scienze Ostetrico-Ginecologiche, Urologiche e Medicina della Riproduzione, Universita` Federico II, Napoli, Italy
Istituto di Endocrinologia ed Oncologia Sperimentale, CNR, Napoli, Italy (literal)
- Titolo
- Inverted duplication of 15q with terminal deletion in a multiple malformed newborn with intrauterine growth failure and lethal phenotype. (literal)
- Abstract
- We describe the cytogenetic and molecular characterization
of an inverted duplication of chromosome
15q with evidence of a terminal deletion of
the same rearranged chromosome. The proband
was a multiple congenital malformed female with
a prenatal diagnosis of trisomy 15q and an extremely
severe clinical course. The phenotype of the
patient was characterized by marked intrauterine
growth retardation, congenital heart defect,
''horseshoe'' kidney, hand contractures, and clubfeet.
The exitus came at 20 days because of progressive
cardio-respiratory impairment. Overall,
the clinical phenotype appeared more severe than
usual trisomy 15q syndrome. Postnatal cytogenetic
and molecular studies unraveled a ''de novo''
inverted duplication of 15q (q21.3!q26.3), associated
with the deletion of the 15q telomere and
part of the band 15q26.3. A single copy region
spanning approximately 600 kb between the
duplicated segments was present. Correlation
between the clinical findings of the patient and
the phenotype of trisomy 15q reported in literature
is also provided. (literal)
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