Literature DB >> 10655752

[A nevoid basal cell carcinoma syndrome with chromosomal aberration].

K Sasaki1, T Yoshimoto, T Nakao, K Minagawa, Y Takahashi, Y Watanabe, C Tanabe.   

Abstract

We reported a boy with nevoid basal cell carcinoma syndrome (NBCCS) with chromosomal aberration. He showed multiple jaw cysts, basal cell carcinomas, hypertelorism, macrocephaly and mental retardation. Cranial CT revealed calcification of the falx cerebri and tentorium cerebelli, and dilatation of the lateral ventricles. MRI showed a thin corpus callosum. A chromosomal study revealed a deletion of 9q21.31-q22.31. He had generalized tonic-clonic seizures, which were well controlled. Since the gene for NBCCS was recently mapped to chromosome 9q22.3, we suspected that the deletion site in this patient was responsible for his symptoms of NBCCS.

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Year:  2000        PMID: 10655752

Source DB:  PubMed          Journal:  No To Hattatsu        ISSN: 0029-0831


  4 in total

1.  Gorlin's syndrome with a thin corpus callosum and a third ventricular cyst.

Authors:  M Kantarci; U Ertas; F Alper; Y Sutbeyaz; R M Karasen; O Onbas
Journal:  Neuroradiology       Date:  2003-05-17       Impact factor: 2.804

2.  9q22 Deletion--first familial case.

Authors:  Linda Siggberg; Maarit Peippo; Marjatta Sipponen; Taina Miikkulainen; Keiko Shimojima; Toshiyuki Yamamoto; Jaakko Ignatius; Sakari Knuutila
Journal:  Orphanet J Rare Dis       Date:  2011-06-22       Impact factor: 4.123

3.  High-density oligonucleotide array with sub-kilobase resolution reveals breakpoint information of submicroscopic deletions in nevoid basal cell carcinoma syndrome.

Authors:  Katsunori Fujii; Shumpei Ishikawa; Hideki Uchikawa; Daisuke Komura; Michael H Shapero; Fan Shen; Jing Hung; Hiroshi Arai; Yoko Tanaka; Kimio Sasaki; Yoichi Kohno; Masao Yamada; Keith W Jones; Hiroyuki Aburatani; Toshiyuki Miyashita
Journal:  Hum Genet       Date:  2007-08-17       Impact factor: 4.132

4.  PTCH mutations and deletions in patients with typical nevoid basal cell carcinoma syndrome and in patients with a suspected genetic predisposition to basal cell carcinoma: a French study.

Authors:  N Soufir; B Gerard; M Portela; A Brice; M Liboutet; P Saiag; V Descamps; D Kerob; P Wolkenstein; I Gorin; C Lebbe; N Dupin; B Crickx; N Basset-Seguin; B Grandchamp
Journal:  Br J Cancer       Date:  2006-08-21       Impact factor: 7.640

  4 in total

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