49,XXXXY综合征中的先天性心脏病。 - Suppr

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超能文献

Congenital heart disease in 49, XXXXY syndrome.

作者信息

Karsh R B

出版信息

Pediatrics. 1975 Sep;56(3):462-4.

PMID:1161403

Abstract

摘要

相似文献

Congenital heart disease in 49, XXXXY syndrome.49,XXXXY综合征中的先天性心脏病。

Pediatrics. 1975 Sep;56(3):462-4.

[49,xxxxy syndrome associated with congenital heart disease (author's transl)].[49，XXXXY综合征合并先天性心脏病（作者译）]

Lijec Vjesn. 1976 Jul;98(7):366-70.

Growth failure in association with congenital heart disease.与先天性心脏病相关的生长发育迟缓。

Pediatr Ann. 1978 Nov;7(11):750-9.

Hypertensive pulmonary vascular disease complicating congenital heart disease. A review.先天性心脏病合并高血压性肺血管疾病。综述。

Cardiovasc Clin. 1973;5(1):43-60.

Pulmonary hypertension in congenital shunt lesions. Observations in a right heart catheterization material, with particular reference to occurrence, natural history and prognostic implications in adolescence and adulthood.先天性分流性病变中的肺动脉高压。右心导管检查资料的观察，特别提及青少年和成年期的发生率、自然史及预后意义。

Acta Med Scand Suppl. 1972;535:3-26.

Hypoplastic genitalia, abnormal facies and congenital heart disease.生殖器发育不全、面容异常和先天性心脏病。

Proc R Soc Med. 1971 Jan;64(1):18-9. doi: 10.1177/003591577106400110.

[Pulmonary hypertension in congenital heart defects in childhood].[儿童先天性心脏病中的肺动脉高压]

Bibl Paediatr. 1967;85:1-89.

[A case of central nervous system anomalies (agenesis of corpus callosum, colpocephaly, hydrocephalus, congenital dermal sinus) associated with congenital heart disease(double-outlet right ventricle, complete endocardial cushion defect, atrial septal defect, pulmonary arterial stenosis, patent ductus arteriosus)].[一例与先天性心脏病（右心室双出口、完全性心内膜垫缺损、房间隔缺损、肺动脉狭窄、动脉导管未闭）相关的中枢神经系统异常（胼胝体发育不全、脑室扩张、脑积水、先天性皮样窦）病例]

No To Shinkei. 2001 Feb;53(2):179-84.

Patent ductus arteriosus, ventricular septal defect and pulmonary hypertension in a child with 49, XXXXY syndrome.

Genet Couns. 2006;17(3):391-3.

Proceedings: Cardiovascular malformations in oesophageal atresia.会议论文：食管闭锁中的心血管畸形

Br Heart J. 1974 Oct;36(10):1036.

引用本文的文献

An infant with 49XXXXY syndrome: a case report.49XXXXY 综合征婴儿 1 例报告

J Med Case Rep. 2021 Dec 30;15(1):630. doi: 10.1186/s13256-021-03188-4.

Identification of novel candidate gene loci and increased sex chromosome aneuploidy among infants with conotruncal heart defects.圆锥动脉干心脏缺陷婴儿中新型候选基因位点的鉴定及性染色体非整倍体增加

Am J Med Genet A. 2014 Feb;164A(2):397-406. doi: 10.1002/ajmg.a.36291. Epub 2013 Oct 11.

49,XXXXY: a distinct phenotype. Three new cases and review.49,XXXXY：一种独特的表型。三例新病例及文献复习

J Med Genet. 1998 May;35(5):420-4. doi: 10.1136/jmg.35.5.420.

Total anomalous origin of the coronary arteries from the pulmonary artery.冠状动脉起源于肺动脉的完全性异常。

Pediatr Cardiol. 1986;7(1):11-8. doi: 10.1007/BF02315476.

Epiphysial dysplasia: a constant finding in the XXXXY syndrome.骨骺发育异常：XXXXY综合征中的一个恒定发现。

J Med Genet. 1978 Aug;15(4):282-7. doi: 10.1136/jmg.15.4.282.

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