Early-onset basal cell carcinoma in a case of Ivemark syndrome

Anna Zampetti; M Gnarra; D Linder; D Antuzzi; L Cataldi; A Tulli; Claudio Feliciani

doi:10.1684/ejd.2010.1093

Early-onset basal cell carcinoma in a case of Ivemark syndrome

Anna Zampetti, M Gnarra, D Linder, D Antuzzi, L Cataldi, A Tulli, Claudio Feliciani

Risultato della ricerca: Contributo in rivista › Articolo in rivista

1 Citazioni (Scopus)

Abstract

First described by the Swedish paediatrician, Björn Ivemark, (1925-2005), IS is a rare congenital heterotaxic disorder with lateralization anomalies [1]. It accounts for 1- 3% of all congenital heart defects, with an incidence of 1 in 10-20,000 live births. To date, about 200 cases have been reported in the literature, mostly sporadic, but familial occurrence has also been described, suggesting autosomal recessive inheritance, with a male preponderance.

Lingua originale	English
pagine (da-a)	845-846
Numero di pagine	2
Rivista	European Journal of Dermatology
Volume	20
DOI	https://doi.org/10.1684/ejd.2010.1093
Stato di pubblicazione	Pubblicato - 2010
Pubblicato esternamente	Sì

Keywords

Abnormalities, Multiple
Carcinoma, Basal Cell
Female
Heart Defects, Congenital
Heterotaxy Syndrome
Humans
Shoulder
Skin Neoplasms
Splenic Diseases
Young Adult

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10.1684/ejd.2010.1093

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title = "Early-onset basal cell carcinoma in a case of Ivemark syndrome",

abstract = "First described by the Swedish paediatrician, Bj{\"o}rn Ivemark, (1925-2005), IS is a rare congenital heterotaxic disorder with lateralization anomalies [1]. It accounts for 1- 3% of all congenital heart defects, with an incidence of 1 in 10-20,000 live births. To date, about 200 cases have been reported in the literature, mostly sporadic, but familial occurrence has also been described, suggesting autosomal recessive inheritance, with a male preponderance.",

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author = "Anna Zampetti and M Gnarra and D Linder and D Antuzzi and L Cataldi and A Tulli and Claudio Feliciani",

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doi = "10.1684/ejd.2010.1093",

language = "English",

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T1 - Early-onset basal cell carcinoma in a case of Ivemark syndrome

AU - Zampetti, Anna

AU - Gnarra, M

AU - Linder, D

AU - Antuzzi, D

AU - Cataldi, L

AU - Tulli, A

AU - Feliciani, Claudio

PY - 2010

Y1 - 2010

N2 - First described by the Swedish paediatrician, Björn Ivemark, (1925-2005), IS is a rare congenital heterotaxic disorder with lateralization anomalies [1]. It accounts for 1- 3% of all congenital heart defects, with an incidence of 1 in 10-20,000 live births. To date, about 200 cases have been reported in the literature, mostly sporadic, but familial occurrence has also been described, suggesting autosomal recessive inheritance, with a male preponderance.

AB - First described by the Swedish paediatrician, Björn Ivemark, (1925-2005), IS is a rare congenital heterotaxic disorder with lateralization anomalies [1]. It accounts for 1- 3% of all congenital heart defects, with an incidence of 1 in 10-20,000 live births. To date, about 200 cases have been reported in the literature, mostly sporadic, but familial occurrence has also been described, suggesting autosomal recessive inheritance, with a male preponderance.

KW - Abnormalities, Multiple

KW - Carcinoma, Basal Cell

KW - Female

KW - Heart Defects, Congenital

KW - Heterotaxy Syndrome

KW - Humans

KW - Shoulder

KW - Skin Neoplasms

KW - Splenic Diseases

KW - Young Adult

KW - Abnormalities, Multiple

KW - Carcinoma, Basal Cell

KW - Female

KW - Heart Defects, Congenital

KW - Heterotaxy Syndrome

KW - Humans

KW - Shoulder

KW - Skin Neoplasms

KW - Splenic Diseases

KW - Young Adult

UR - http://hdl.handle.net/10807/42930

U2 - 10.1684/ejd.2010.1093

DO - 10.1684/ejd.2010.1093

M3 - Article

SN - 1167-1122

VL - 20

SP - 845

EP - 846

JO - European Journal of Dermatology

JF - European Journal of Dermatology

ER -

Early-onset basal cell carcinoma in a case of Ivemark syndrome

Abstract

Keywords

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