Literature DB >> 15717176

Early recognition of basal cell naevus syndrome.

Hermine E Veenstra-Knol1, Jan H Scheewe, Gerrit J van der Vlist, Menno E van Doorn, Margreet G E M Ausems.   

Abstract

UNLABELLED: The basal cell naevus syndrome is an autosomal dominant syndrome characterised by major manifestations such as basal cell carcinomas, jaw cysts, palmar or plantar pits, and intracranial calcifications. Early recognition is important in order to reduce morbidity due to cutaneous and cerebral malignancy and oromaxillofacial deformation and destruction, although diagnosis in infancy is rare. We describe three unrelated children with basal cell naevus syndrome who appeared to be the first patient in each family.
CONCLUSION: Our observations lead us to recommend looking for other manifestations of this disease in patients who present with cardiac fibroma, cleft lip/palate, polydactyly or macrocephaly. Bifid, fused or splayed ribs should be considered a major criterion of great help in establishing a diagnosis, particularly in young children.

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Year:  2004        PMID: 15717176     DOI: 10.1007/s00431-004-1597-4

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  12 in total

1.  Basal cell nevus syndrome: guidelines for early detection.

Authors:  George J Bitar; Charles K Herman; Mohammed I Dahman; Martin A Hoard
Journal:  Am Fam Physician       Date:  2002-06-15       Impact factor: 3.292

2.  Human homolog of patched, a candidate gene for the basal cell nevus syndrome.

Authors:  R L Johnson; A L Rothman; J Xie; L V Goodrich; J W Bare; J M Bonifas; A G Quinn; R M Myers; D R Cox; E H Epstein; M P Scott
Journal:  Science       Date:  1996-06-14       Impact factor: 47.728

Review 3.  Nevoid basal cell carcinoma syndrome: review of 118 affected individuals.

Authors:  S Shanley; J Ratcliffe; A Hockey; E Haan; C Oley; D Ravine; N Martin; C Wicking; G Chenevix-Trench
Journal:  Am J Med Genet       Date:  1994-04-15

4.  De novo mutations of the Patched gene in nevoid basal cell carcinoma syndrome help to define the clinical phenotype.

Authors:  C Wicking; S Gillies; I Smyth; S Shanley; L Fowles; J Ratcliffe; B Wainwright; G Chenevix-Trench
Journal:  Am J Med Genet       Date:  1997-12-19

Review 5.  Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome.

Authors:  V E Kimonis; A M Goldstein; B Pastakia; M L Yang; R Kase; J J DiGiovanna; A E Bale; S J Bale
Journal:  Am J Med Genet       Date:  1997-03-31

6.  Complications of the naevoid basal cell carcinoma syndrome: results of a population based study.

Authors:  D G Evans; E J Ladusans; S Rimmer; L D Burnell; N Thakker; P A Farndon
Journal:  J Med Genet       Date:  1993-06       Impact factor: 6.318

Review 7.  Nevoid basal-cell carcinoma syndrome.

Authors:  R J Gorlin
Journal:  Medicine (Baltimore)       Date:  1987-03       Impact factor: 1.889

Review 8.  Nevoid basal cell carcinoma syndrome: a review of the literature.

Authors:  M Manfredi; P Vescovi; M Bonanini; S Porter
Journal:  Int J Oral Maxillofac Surg       Date:  2004-03       Impact factor: 2.789

9.  Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome.

Authors:  H Hahn; C Wicking; P G Zaphiropoulous; M R Gailani; S Shanley; A Chidambaram; I Vorechovsky; E Holmberg; A B Unden; S Gillies; K Negus; I Smyth; C Pressman; D J Leffell; B Gerrard; A M Goldstein; M Dean; R Toftgard; G Chenevix-Trench; B Wainwright; A E Bale
Journal:  Cell       Date:  1996-06-14       Impact factor: 41.582

10.  Spectrum of PTCH1 mutations in French patients with Gorlin syndrome.

Authors:  Nathalie Boutet; Yves-Jean Bignon; Valérie Drouin-Garraud; Pierre Sarda; Michel Longy; Didier Lacombe; Philippe Gorry
Journal:  J Invest Dermatol       Date:  2003-09       Impact factor: 8.551

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  13 in total

1.  Basal cell nevus syndrome: clinical and genetic diagnosis.

Authors:  José A García de Marcos; Alicia Dean-Ferrer; Susana Arroyo Rodríguez; Javier Calderón-Polanco; Francisco J Alamillos Granados; Enrique Poblet
Journal:  Oral Maxillofac Surg       Date:  2009-12

2.  Co-occurrence of mutations in FOXP1 and PTCH1 in a girl with extreme megalencephaly, callosal dysgenesis and profound intellectual disability.

Authors:  Melinda Zombor; Tibor Kalmár; Zoltán Maróti; Alíz Zimmermann; Adrienn Máté; Csaba Bereczki; László Sztriha
Journal:  J Hum Genet       Date:  2018-09-04       Impact factor: 3.172

Review 3.  Gorlin-Goltz syndrome--a medical condition requiring a multidisciplinary approach.

Authors:  Małgorzata Kiwilsza; Katarzyna Sporniak-Tutak
Journal:  Med Sci Monit       Date:  2012-09

4.  A case report of Gorlin-Goltz syndrome as a rare hereditary disorder.

Authors:  Mehri Sirous; Nazila Tayari
Journal:  J Res Med Sci       Date:  2011-06       Impact factor: 1.852

5.  [Gorlin-Goltz syndrome-not just a syndrome of malignant eyelid tumors].

Authors:  C Kortuem; A Abaza; C Schramm; F Kortuem
Journal:  Ophthalmologe       Date:  2021-03-26       Impact factor: 1.059

6.  Incidental finding of lamellar calcification of the falx cerebri leading to the diagnosis of gorlin-goltz syndrome.

Authors:  I Saulite; B Voykov; T Mehra; W Hoetzenecker; E Guenova
Journal:  Case Rep Dermatol       Date:  2013-10-19

7.  Basal cell nevus syndrome (Gorlin-Goltz syndrome): genetic predisposition, clinical picture and treatment.

Authors:  Henryk Witmanowski; Paweł Szychta; Katarzyna Błochowiak; Arkadiusz Jundziłł; Rafał Czajkowski
Journal:  Postepy Dermatol Alergol       Date:  2017-08-02       Impact factor: 1.837

8.  Gorlin-Goltz syndrome: incidental finding on routine ct scan following car accident.

Authors:  Christina Kalogeropoulou; Petros Zampakis; Santra Kazantzi; Pantelis Kraniotis; Nicholas S Mastronikolis
Journal:  Cases J       Date:  2009-11-25

9.  Nevoid basal cell carcinoma syndrome (Gorlin-Goltz syndrome).

Authors:  N K Kiran; T N Tilak Raj; K S Mukunda; V Rajashekar Reddy
Journal:  Contemp Clin Dent       Date:  2012-10

10.  Gorlin-Goltz Syndrome: Case report and literature review.

Authors:  Maya Ramesh; Ramesh Krishnan; Paul Chalakkal; George Paul
Journal:  J Oral Maxillofac Pathol       Date:  2015 May-Aug
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