Mitral valve repair in a patient with ter Haar syndrome

被引：2

作者：

Barlas, Semih

Ugurlucan, Murat

Ayhan, Yusuf I.

Kalangos, Afksendyios

Barlas, Cemil

机构：

[1] Istanbul Fac Med, Dept Cardiovasc Surg, TR-34728 Istanbul, Turkey

[2] German Hosp, Univ Hosp Grp, Dept Pediat Cardiac Surg, Istanbul, Turkey

来源：

JOURNAL OF CARDIAC SURGERY | 2006年 / 21卷 / 05期

关键词：

D O I：

10.1111/j.1540-8191.2006.00306.x

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Ter Haar Syndrome is one of the most deteriorating disorders defined in the medical era. Up to date only ten patients were reported. We present a living patient with ter Haar Syndrome who has undergone successful mitral valve repair.

引用

页码：488 / 491

页数：4

共 9 条

[1] Siblings with glaucoma, mental retardation and short stature [J].

AlKaissi, A ;

Hammou, A ;

Ben Ghachem, M ;

Nacib, MN ;

Ben Chehida, F ;

Karoui, H ;

Baraitser, M .

CLINICAL DYSMORPHOLOGY, 2003, 12 (03) :191-194

[2] BOWEN SYNDROME - CONGENITAL GLAUCOMA, FLEXION CONTRACTURE OF FINGERS AND FACIAL DYSMORPHISM WITHOUT PEROXISOMAL ABNORMALITIES [J].

DEVILLEMEUR, TB ;

BIJAOUI, G ;

BEAUVAIS, P ;

RICHARDET, JM .

EUROPEAN JOURNAL OF PEDIATRICS, 1992, 151 (02) :146-147

[3] AUTOSOMAL RECESSIVE MELNICK-NEEDLES SYNDROME OR TER HAAR SYNDROME - REPORT OF A PATIENT AND REAPPRAISAL OF AN EARLIER REPORT [J].

HAMEL, BCJ ;

DRAAISMA, JMT ;

PINCKERS, AJLG ;

BOETES, C ;

HOPPE, RLE ;

ROPERS, HH ;

BRUNNER, HG .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 56 (03) :312-316

[4] Further delineation of Frank-ter Haar syndrome [J].

Maas, SM ;

Kayserili, H ;

Lam, J ;

Apak, MY ;

Hennekam, RCM .

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 131A (02) :127-133

[5]

Megarbane A, 1997, AM J MED GENET, V73, P67, DOI 10.1002/(SICI)1096-8628(19971128)73:1<67::AID-AJMG13>3.0.CO

[6]

2-P

[7] MELNICK-NEEDLES SYNDROME - INDICATION FOR AN AUTOSOMAL RECESSIVE FORM [J].

TERHAAR, B ;

HAMEL, B ;

HENDRIKS, J ;

DEJAGER, J .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 13 (04) :469-477

[8]

Wallerstein R, 1997, AM J MED GENET, V70, P267, DOI 10.1002/(SICI)1096-8628(19970613)70:3<267::AID-AJMG10>3.0.CO

[9]

2-J

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