scholarly journals Sirenomelia with Potter syndrome: a case report and review of literature

2019 ◽  
Vol 9 (1) ◽  
pp. 400
Author(s):  
Amrita Singh ◽  
Anupma Kumari
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Prenatal Diagnosis ◽  
Lower Extremities ◽  
Rare Condition ◽  
Variable Degree ◽  
Review Of Literature ◽  
Rare Congenital Anomaly ◽  
Mermaid Syndrome ◽  
Vascular Steal

Sirenomelia or mermaid syndrome is a rare congenital anomaly characterized by variable degree of fusion of lower extremities. Awareness to this rare condition is important for prenatal diagnosis and prognosticating the fetus. The exact etiopathogenesis is still an area of research. Two pathogenic hypotheses are the vascular steal hypothesis and the defective blastogenesis hypothesis with exceptions reported in literature.

CONGENITAL METACARPAL SYNOSTOSIS TREATED BY DOUBLE BONE BLOCKS TECHNIQUE: A CASE REPORT FROM THAILAND

Hand Surgery ◽  
2005 ◽  
Vol 10 (01) ◽  
pp. 131-134 ◽  
Author(s):  
Surut Jianmongkol ◽  
Tala Thammaroj ◽  
Kitiwan Vipulakorn
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Surgical Techniques ◽  
Rare Condition ◽  
Rare Congenital Anomaly

Congenital metacarpal synostosis is a rare congenital anomaly in the hand, especially in our area. There were several reports of surgical techniques for correction deformities. We report this rare condition in our hospital and treatment with the metacarpal osteotomy and double bone blocks technique of grafting.

scholarly journals Rare presentation of incomplete male urethral duplication: A case report and review of literature

2021 ◽  
Vol 9 (1) ◽  
pp. 292-296
Author(s):  
Orgeness J Mbwambo ◽  
Alex Mremi ◽  
Mohamed Mbarouk ◽  
Jasper Mbwambo ◽  
Frank Bright ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Postoperative Period ◽  
Surgical Removal ◽  
Urethral Duplication ◽  
Review Of Literature ◽  
Rare Presentation ◽  
Rare Congenital Anomaly ◽  
Accessory Urethra

Urethral duplication is a rare congenital anomaly affecting mainly males. Here, we report a case of urethral duplication in a 19 years old male presented as a scrotal sinus discharging pus for 1 year. Surgical removal of accessory urethra was done and postoperative period was uneventful.

scholarly journals Sirenomelia: A Case Report of a Rare Congenital Anomaly and Review of Literature

2016 ◽  
Vol 02 (01) ◽  
pp. 030-032
Author(s):  
Mohammad Khan ◽  
Pallavi Todase
Keyword(s):  
Congenital Anomaly ◽  
Umbilical Artery ◽  
Review Of Literature ◽  
Single Umbilical Artery ◽  
Rare Congenital Anomaly ◽  
Limb Bones ◽  
Mermaid Syndrome ◽  
First Case ◽  
Renal Abnormalities ◽  
Dysplastic Kidneys

AbstractSirenomelia, or the Mermaid Syndrome, is a very rare congenital anomaly. It is associated with varying degrees of fusion of lower limb bones, giving them the appearance of a “mermaid.” It is almost always associated with other birth defects, such as, renal abnormalities, genital anomalies, and cardiac anomalies. We report a case of sirenomelia associated with bilateral multicystic dysplastic kidneys along with bilateral hydronephrosis, severe oligohydramnios, single umbilical artery, absent anal opening, and absent genitals. To the best of our knowledge, this is the first case to be reported from our region.

scholarly journals Klippel-Feil Syndrome: A Review of Literature and Case Report

2018 ◽  
Vol 1 (1) ◽  
pp. 102-107
Author(s):  
H Mohammad ◽  
I T Annongu ◽  
D D Mue ◽  
D M Chia ◽  
R O Abah ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Review Of Literature ◽  
Rare Congenital Anomaly ◽  
Clinical Presentations ◽  
Complete History ◽  
Radiological Examinations

Though Klippel-Feil syndrome is a rare congenital anomaly and the clinical presentations are varied, a complete history, physical and radiological examinations may reveal the diagnosis.

scholarly journals Macrodystrophia Lipomatosa- A Rare Congenital Anomaly: A Case Report and Review of Literature

2016 ◽  
Vol 2 (5) ◽  
Author(s):  
Sanjay Kumar Tripathi ◽  
Saurav Narayan Nanda ◽  
Shalesh kumar ◽  
Nitin kumar Agrawal ◽  
Shaikh Muzammil Shiraz ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Review Of Literature ◽  
Rare Congenital Anomaly ◽  
Macrodystrophia Lipomatosa

scholarly journals A rare case of double gall bladder: a case report and review of literature

2021 ◽  
Vol 8 (11) ◽  
pp. 3488
Author(s):  
Gurushantappa Yalagachin ◽  
Abhijit D. Hiregoudar ◽  
Ashika Bagur ◽  
Abhishek Choudhari
Keyword(s):  
Congenital Anomaly ◽  
Laparoscopic Cholecystectomy ◽  
Case Report ◽  
Gall Bladder ◽  
Preoperative Diagnosis ◽  
Rare Case ◽  
Review Of Literature ◽  
Rare Congenital Anomaly ◽  
Hepatobiliary System ◽  
Double Gallbladder

Double gall bladder is a rare congenital anomaly of the Hepatobiliary system with an incidence of 1:4000 due to abnormalities resulting during the embryogenesis during fourth to sixth week of gestation. Boyden was first to describe the duplication of the gallbladder and Harlaftis classification describes three types for the duplication of the gallbladder. Preoperative diagnosis of the duplication of the gallbladder has to be confirmed to minimise the complications during the surgery and post operatively. Sometimes the duplication of the gallbladder is missed preoperatively and hence increasing the risk and complications during the cholecystectomy. MRCP is the investigation of choice for preoperative diagnosis of the duplication and the laparoscopic cholecystectomy being the treatment of choice for the double gallbladder. We encountered a 25 year old girl with duplicate gallbladder who underwent laparoscopic cholecystectomy with removal of both gallbladders successfully.

Prenatal diagnosis of trisomy 1q21-qter: Case report and review of literature

2005 ◽  
Vol 134A (2) ◽  
pp. 207-211 ◽  
Author(s):  
Andrea Machlitt ◽  
Peter Kuepferling ◽  
Christiane Bommer ◽  
Hannelore Koerner ◽  
Rabih Chaoui
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Review Of Literature

Prenatal diagnosis of Pfeiffer syndrome and role of three-dimensional ultrasound: case report and review of literature

2021 ◽  
pp. 1-4
Author(s):  
Antonella Vimercati ◽  
Claudiana Olivieri ◽  
Miriam Dellino ◽  
Mattia Gentile ◽  
Raffaele Tinelli ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Three Dimensional ◽  
Review Of Literature ◽  
Pfeiffer Syndrome

scholarly journals Incidental Finding of Annular Pancreas in a Routine Cadaveric Dissection: Case Report

2019 ◽  
Vol 36 (04) ◽  
pp. 299-302
Author(s):  
Mythraeyee Prasad ◽  
Theresa Susan Kuriakose ◽  
Sipra Rout
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Duodenal Obstruction ◽  
Clinical Symptoms ◽  
Incidental Finding ◽  
Age Groups ◽  
Annular Pancreas ◽  
Present Case Report ◽  
Rare Congenital Anomaly ◽  
Variable Presentation

AbstractAnnular pancreas is a rare congenital anomaly that results from the malrotation of the ventral pancreatic bud. The presentation of annular pancreas varies: it can be asymptomatic or present clinical symptoms of duodenal obstruction that can affect all age groups, from newborns to adults. In the present case report, we describe a complete type of annular pancreas at the level of the second part of the duodenum, which was an incidental finding in a prosected specimen. This anomaly has significant clinical relevance to clinicians and radiologists due to its variable presentation. The embryological, clinical and radiological aspects of this congenital anomaly are discussed in detail in the present article.

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