一种累及心脏、皮肤和内分泌系统的新型遗传性综合征。 - Suppr | 超能文献

A new inherited syndrome with cardiac, cutaneous, and endocrine involvement.

作者信息

Michels V V

出版信息

Mayo Clin Proc. 1986 Mar;61(3):224-5. doi: 10.1016/s0025-6196(12)61854-0.

DOI:10.1016/s0025-6196(12)61854-0

Abstract

摘要

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

文档翻译

学术文献翻译模型，支持多种主流文档格式。

相似文献

1

A new inherited syndrome with cardiac, cutaneous, and endocrine involvement.一种累及心脏、皮肤和内分泌系统的新型遗传性综合征。

Mayo Clin Proc. 1986 Mar;61(3):224-5. doi: 10.1016/s0025-6196(12)61854-0.

2

Autosomal dominant transmission of the NAME syndrome (nevi, atrial myxoma, mucinosis of the skin and endocrine overactivity).

Hum Genet. 1991 Jan;86(3):300-4. doi: 10.1007/BF00202415.

3

The Carney complex (myxomas, spotty pigmentation, endocrine overactivity, and schwannomas).卡尼综合征（黏液瘤、斑点状色素沉着、内分泌功能亢进及神经鞘瘤）。

Dermatol Clin. 1995 Jan;13(1):19-26.

4

Cutaneous myxomas. A major component of the complex of myxomas, spotty pigmentation, and endocrine overactivity.皮肤黏液瘤。黏液瘤、散在色素沉着和内分泌功能亢进综合征的主要组成部分。

Arch Dermatol. 1986 Jul;122(7):790-8. doi: 10.1001/archderm.122.7.790.

5

[The myxoma syndrome: "cardiac myxoma, cutaneous pigmented lesions and peripheral and endocrine neoplasms". Apropos 2 cases].[黏液瘤综合征：“心脏黏液瘤、皮肤色素沉着病变及周围和内分泌肿瘤”。附2例报告]

Rev Esp Cardiol. 1994 Feb;47(2):113-5.

6

A familial syndrome of cardiac myxomas, myxoid neurofibromata, cutaneous pigmented lesions, and endocrine abnormalities.

Aust N Z J Med. 1986 Jun;16(3):393-6. doi: 10.1111/j.1445-5994.1986.tb01196.x.

7

Familial cardiac myxoma: Carney's complex.家族性心脏黏液瘤：卡尼综合征。

Tex Heart Inst J. 2003;30(1):80-2.

8

Carney complex: a case report.卡尼综合征：一例病例报告。

Rev Port Cardiol. 2009 Feb;28(2):211-22.

9

Cutaneous and cardiac myxomas: an important association.皮肤和心脏黏液瘤：一种重要的关联。

Semin Dermatol. 1991 Sep;10(3):148-51.

10

[Association of cardiac myxomas and pigmented cutaneous lesions: a new cardiocutaneous syndrome?].

Ann Dermatol Venereol. 1986;113(12):1279-81.

引用本文的文献

1

The role of genetic and epigenetic changes in pituitary tumorigenesis.基因和表观遗传变化在垂体肿瘤发生中的作用。

Neurol Med Chir (Tokyo). 2014;54(12):943-57. doi: 10.2176/nmc.ra.2014-0184. Epub 2014 Nov 29.

2

Mutations in regulatory subunit type 1A of cyclic adenosine 5'-monophosphate-dependent protein kinase (PRKAR1A): phenotype analysis in 353 patients and 80 different genotypes.环磷酸腺苷依赖性蛋白激酶1A型调节亚基（PRKAR1A）的突变：353例患者的表型分析及80种不同基因型

J Clin Endocrinol Metab. 2009 Jun;94(6):2085-91. doi: 10.1210/jc.2008-2333. Epub 2009 Mar 17.