Literature DB >> 10066029

Nevoid basal cell carcinoma syndrome. Clinical findings in 37 Italian affected individuals.

L Lo Muzio1, P F Nocini, A Savoia, U Consolo, M Procaccini, L Zelante, G Pannone, P Bucci, M Dolci, F Bambini, P Solda, G Favia.   

Abstract

Nevoid basal cell carcinoma syndrome (NBCCS) is a hereditary condition transmitted as an autosomal dominant trait with complete penetrance and variable expressivity. The syndrome is characterised by numerous basal cell carcinomas (BCCs), odontogenic keratocysts of the jaws, palmar and/or plantar pits, skeletal abnormalities and intracranial calcifications. In this paper, the clinical features of 37 Italian patients are reviewed. Jaw cysts and calcification of falx cerebri were the most frequently observed anomalies, followed by BCCs and palmar/plantar pits. Similar to the case of African Americans, the relatively low frequency of BCCs in the Italian population is probably due to protective skin pigmentation. A future search based on mutation screening might establish a possible genotype phenotype correlation in Italian patients.

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Year:  1999        PMID: 10066029     DOI: 10.1034/j.1399-0004.1999.550106.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  40 in total

1.  Multiple palmar pits and basal cell carcinomas.

Authors:  José Juan Pereyra-Rodríguez; José Bernabeu-Wittel; Julián Conejo-Mir
Journal:  CMAJ       Date:  2010-05-25       Impact factor: 8.262

2.  [Calcification of the falx cerebri. A pathognomonic symptom of Gorlin-Goltz syndrome].

Authors:  J T Lambrecht; S Stübinger; B Siewert; F Härle
Journal:  HNO       Date:  2005-08       Impact factor: 1.284

3.  Clinical utility gene card for: Gorlin syndrome.

Authors:  Lorenzo Lo Muzio; Lorenza Pastorino; Sonja Levanat; Vesna Musani; Mima Situm; Giovanna Bianchi Scarra
Journal:  Eur J Hum Genet       Date:  2011-02-09       Impact factor: 4.246

4.  Gorlin-Goltz syndrome: first reported case of bullae in the lungs complicated with tension pneumothorax.

Authors:  Darren Yap
Journal:  BMJ Case Rep       Date:  2018-06-20

5.  Clinical utility gene card for: Gorlin syndrome--update 2013.

Authors:  Lorenzo Lo Muzio; Lorenza Pastorino; Sonja Levanat; Vesna Musani; Mima Situm; Giovanni Ponti; Giovanna Bianchi Scarra
Journal:  Eur J Hum Genet       Date:  2013-01-30       Impact factor: 4.246

6.  Neurocutaneous melanocytosis, hemimegalencephaly and large ovarian cyst in a newborn.

Authors:  Betul E Derinkuyu; Oznur Boyunaga; Sezin Unal; Murat Ucar; Ebru Ergenekon
Journal:  Pediatr Radiol       Date:  2015-02-17

7.  Syndrome in question: Gorlin-Goltz syndrome.

Authors:  Pauline Lyrio Ribeiro; João Basílio de Souza; Karina Demoner de Abreu; Marisa Simon Brezinscki; Christine Chambo Pignaton
Journal:  An Bras Dermatol       Date:  2016 Jul-Aug       Impact factor: 1.896

8.  Keratocystic odontogenic tumors related to Gorlin-Goltz syndrome: A clinicopathological study.

Authors:  Mohammed Israr Ul Khaliq; Ajaz A Shah; Irshad Ahmad; Shahid Hasan; Sagar S Jangam
Journal:  J Oral Biol Craniofac Res       Date:  2015-11-11

Review 9.  Nevoid basal cell carcinoma syndrome (Gorlin syndrome).

Authors:  Lorenzo Lo Muzio
Journal:  Orphanet J Rare Dis       Date:  2008-11-25       Impact factor: 4.123

10.  Neuroimaging of nevoid basal cell carcinoma syndrome (NBCCS) in children.

Authors:  Kamyar Sartip; Adam Kaplan; George Obeid; Nadja Kadom
Journal:  Pediatr Radiol       Date:  2012-11-14
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