一名患有基底细胞痣综合征且存在9号染色体q22间质缺失的患者发生的侵袭性基底细胞癌。 - Suppr

Destructive basal cell carcinoma in a patient with basal cell nevus syndrome and an interstitial deletion of chromosome 9q22.

作者信息

Mosterd Klara, Sommer Anja, van Marion Arienne, Lacko Martin, Herbergs Jos, de Bondt Bert Jan, van Steensel Maurice A M, Kelleners-Smeets Nicole W J

出版信息

Dermatol Surg. 2009 Dec;35(12):2051-3. doi: 10.1111/j.1524-4725.2009.01373.x.

DOI:10.1111/j.1524-4725.2009.01373.x

PMID:20050151

Abstract

摘要

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Destructive basal cell carcinoma in a patient with basal cell nevus syndrome and an interstitial deletion of chromosome 9q22.一名患有基底细胞痣综合征且存在9号染色体q22间质缺失的患者发生的侵袭性基底细胞癌。

Dermatol Surg. 2009 Dec;35(12):2051-3. doi: 10.1111/j.1524-4725.2009.01373.x.

Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome.基底细胞痣综合征中间质性9q22缺失的描绘

Am J Med Genet A. 2005 Jan 30;132A(3):324-8. doi: 10.1002/ajmg.a.30422.

Further delineation of 9q22 deletion syndrome associated with basal cell nevus (Gorlin) syndrome: report of two cases and review of the literature.与基底细胞痣（戈林）综合征相关的9q22缺失综合征的进一步描述：两例报告及文献复习

Congenit Anom (Kyoto). 2009 Mar;49(1):8-14. doi: 10.1111/j.1741-4520.2008.00212.x.

Palmar basal cell carcinoma in a patient with Gorlin-Goltz syndrome.一名患有基底细胞痣综合征患者的手掌部基底细胞癌。

Arch Dermatol. 2007 Jun;143(6):813-4. doi: 10.1001/archderm.143.6.813.

Parental origin of chromosome 9q22.3-q31 lost in basal cell carcinomas from basal cell nevus syndrome patients.基底细胞痣综合征患者基底细胞癌中缺失的9号染色体q22.3 - q31的亲本来源。

Hum Mol Genet. 1994 Mar;3(3):447-8. doi: 10.1093/hmg/3.3.447.

Nevoid basal cell carcinoma syndrome. A review and case report of a patient with unilateral basal cell nevus syndrome.痣样基底细胞癌综合征。单侧基底细胞痣综合征患者的病例报告及文献综述。

J Am Acad Dermatol. 1986 Nov;15(5 Pt 1):1023-30.

The roots of the naevoid basal cell carcinoma syndrome.

Clin Exp Dermatol. 1980 Sep;5(3):339-48. doi: 10.1111/j.1365-2230.1980.tb01712.x.

9q22.3 Microdeletion Syndrome with Multiple Basal Cell Carcinomas Treated with Vismodegib: Three Key Messages in One Patient.9q22.3微缺失综合征合并多发性基底细胞癌经维莫德吉治疗：一例患者的三个关键信息

Acta Derm Venereol. 2018 Feb 7;98(2):287-288. doi: 10.2340/00015555-2822.

Differential allele loss on chromosome 9q22.3 in human non-melanoma skin cancer.人类非黑色素瘤皮肤癌中9号染色体q22.3区域的差异等位基因缺失。

Br J Cancer. 1996 Jul;74(2):246-50. doi: 10.1038/bjc.1996.345.

Interstitial deletion 9q22.32-q33.2 associated with additional familial translocation t(9;17)(q34.11;p11.2) in a patient with Gorlin-Goltz syndrome and features of Nail-Patella syndrome.间质缺失9q22.32-q33.2，伴有额外的家族性易位t(9;17)(q34.11;p11.2)，见于一名患有戈林-戈尔茨综合征且有指甲-髌骨综合征特征的患者。

Am J Med Genet A. 2004 Jan 15;124A(2):179-91. doi: 10.1002/ajmg.a.20367.

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De Novo Interstitial Deletion of 9q in a Pediatric Patient With Global Developmental Delay.一名患有全面发育迟缓的儿科患者出现9号染色体长臂的新发间质性缺失。

Child Neurol Open. 2019 May 7;6:2329048X19844920. doi: 10.1177/2329048X19844920. eCollection 2019.

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Destructive basal cell carcinoma in a patient with basal cell nevus syndrome and an interstitial deletion of chromosome 9q22.

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