痣样基底细胞癌综合征家系1例
痣样基底细胞癌综合征是一种罕见的常染色体显性遗传病，以发育异常和肿瘤发生为主要临床特征。本文报告1例痣样基底细胞癌综合征家系，并结合相关文献对该病的发病率、发病机制、临床表现、治疗方法等进行讨论。
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| Veröffentlicht in: | Hua xi kou qiang yi xue za zhi 2008, Vol.26 (1), p.109-111 |
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| Sprache: | chi |
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| container_title | Hua xi kou qiang yi xue za zhi |
| container_volume | 26 |
| creator | 周晌辉 李力力 翦新春 蒋灿华 |
| description | 痣样基底细胞癌综合征是一种罕见的常染色体显性遗传病，以发育异常和肿瘤发生为主要临床特征。本文报告1例痣样基底细胞癌综合征家系，并结合相关文献对该病的发病率、发病机制、临床表现、治疗方法等进行讨论。 |
| doi_str_mv | 10.3321/j.issn:1000-1182.2008.01.029 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 1000-1182 |
| ispartof | Hua xi kou qiang yi xue za zhi, 2008, Vol.26 (1), p.109-111 |
| issn | 1000-1182 |
| language | chi |
| recordid | cdi_wanfang_journals_hxkqyxzz200801029 |
| source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
| subjects | 家系 牙源性角化囊肿 痣样基底细胞癌综合征 |
| title | 痣样基底细胞癌综合征家系1例 |
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