SIRENOMELIA: THE MERMAID SYNDROME

被引:0
|
作者
Gul, Zahid [1 ]
Jan, Anwar Zeb [1 ]
Liaqat, Fahad [1 ]
Khan, Huma Ambreen [1 ]
机构
[1] Rehman Med Inst, Dept Pediat, Peshawar, Pakistan
来源
GOMAL JOURNAL OF MEDICAL SCIENCES | 2013年 / 11卷 / 01期
关键词
Sirenomelia; Caudal regression syndrome;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sirenomelia (the Mermaid Syndrome) is a rare and lethal congenital anomaly with an incidence of one in 100,000 of normal pregnancies. It is an extremely rare set of birth defects, which can vary in expression. The condition gets its name from one of the defects present, which is a fusing of the legs. The fused nature of the legs has been compared to a mermaid in appearance, hence the name. The characteristic features of Sirenomelia are complete fusion of the lower limbs, commonly associated with renal agenesis, absent external genitalia and other gastrointestinal defects. Another pathognomonic finding is the presence of single umbilical, persistent vitelline artery which is the chief distinguishing anatomic finding from Caudal Regression Syndrome. The termination of pregnancy is the choice of management as the case is diagnosed on the antenatal ultrasound which can show the features like renal agenesis with no liquor, fusion of the lower limbs. In our case report, the baby was delivered through Normal Vaginal Delivery with characteristic features of Sirenomelia on examination. The baby expired 8 hours after delivery.
引用
收藏
页码:114 / 116
页数:3
相关论文
共 50 条
  • [31] CAUDAL REGRESSION - A REVIEW OF 7 CASES, INCLUDING THE MERMAID SYNDROME
    GUIDERA, KJ
    RANEY, E
    OGDEN, JA
    HIGHHOUSE, M
    HABAL, M
    JOURNAL OF PEDIATRIC ORTHOPAEDICS, 1991, 11 (06) : 743 - 747
  • [32] SIRENOMELIA AND ANENCEPHALY
    RODRIGUEZ, JI
    PALACIOS, J
    RAZQUIN, S
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1991, 39 (01): : 25 - 27
  • [33] Sirenomelia: Case Reports and Current Concepts of Pathogenesis
    Pillay, Minnie
    Yesodharan, Dhanya
    Narayanan, Dhanya Lakshmi
    Jojo, Annie
    Luiz, Newton
    Nampoothiri, Sheela
    PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 2012, 15 (05) : 403 - 406
  • [34] Prenatal diagnosis of caudal regression with heterotaxy syndrome: "A mermaid with a broken heart"
    Zhang, Yanhong
    Sun, Congxin
    Jiang, Caixia
    Zhao, Wei
    Wang, Weijing
    Cao, Qingying
    Ge, Shuping
    ECHOCARDIOGRAPHY-A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES, 2019, 36 (02): : 415 - 418
  • [35] PRENATAL SONOGRAPHIC DETECTION OF SYMELIC BIPODIA SIRENOMELIA
    BROOKSHIREQUINN, C
    JEANTY, P
    JOURNAL OF DIAGNOSTIC MEDICAL SONOGRAPHY, 1990, 6 (02) : 103 - 105
  • [36] Sirenomelia: A new type, Showing VACTERL Association with thomas syndrome and a review of literature
    Lhuaire, Martin
    Jestin, Agnes
    Boulagnon, Camille
    Loock, Melanie
    Doco-Fenzy, Martine
    Gaillard, Dominique
    Diebold, Marie-Daniele
    Avisse, Claude
    Labrousse, Marc
    BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, 2013, 97 (03) : 123 - 132
  • [37] Tale of a mermaid
    Vasisht, Pranjali
    Madakshira, Manoj G.
    Kakkar, Nandita
    Singla, Veenu
    Jain, Vanita
    INDIAN JOURNAL OF PATHOLOGY AND MICROBIOLOGY, 2019, 62 (04) : 611 - 613
  • [38] Sirenomelia-Challenges and Treatment Approach in a Rare Case
    Sosinska, Daria
    Golebiewski, Andrzej
    Czauderna, Piotr
    BIRTH DEFECTS RESEARCH, 2024, 116 (12):
  • [39] SIRENOMELIA: A CASE REPORT
    Wankhede, S. K.
    Shrivastava, S.
    JOURNAL OF EVOLUTION OF MEDICAL AND DENTAL SCIENCES-JEMDS, 2016, 5 (14): : 677 - 679
  • [40] Sirenomelia: A case report
    Tamene, Ayanaw
    Molla, Mandefro
    SAGE OPEN MEDICAL CASE REPORTS, 2022, 10