Congenital defects / diseases

Jarcho-Levin Syndrome with Splenic Herniation: A Rare Presentation

Namita Chandra, Sanjay Kumar, Vaibhav Raj, Pawan Kumar Vishwakarma, Sheela Sinha, Ram Prakash Saha

Am J Case Rep 2016; 17:745-748 :: DOI: 10.12659/AJCR.898165

Keywords: Abnormalities, Multiple - diagnosis, Hernia - diagnosis, Hernia, Diaphragmatic - diagnosis, Infant, Newborn, Spleen - diagnostic imaging, Splenic Diseases - diagnosis, Whole Body Imaging - methods

Published: 2016-10-14, Viewed (1280), Downloaded (18), Related (14), Cited (1)

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Diagnosis and Treatment of Small Bowel Strangulation Due To Congenital Band: Three Cases of Congenital Band in Adults Lacking a History of Trauma or Surgery

Gregory Nicolas, Tony Kfoury, Rasha Shimlati, Elliott Koury, Maroon Tohmeh, Elie Gharios, Raja Wakim

Am J Case Rep 2016; 17:712-719 :: DOI: 10.12659/AJCR.899664

Keywords: general surgery, Hand-Assisted Laparoscopy, Laparotomy

Published: 2016-10-07, Viewed (2936), Downloaded (67), Related (8)

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Angioimmunoblastic T-Cell Lymphoma in a Patient with Klinefelter Syndrome

Yong Tae Park, Chan-Ho Park, Mi Ae Bae, Hwa Sik Jung, Youn Im Lee, Ji-Hun Lim, Hee Jeong Cha, Min Jung Seo, Seol Hoon Park, Yunsuk Choi, Hawk Kim, Jae-Cheol Jo

Am J Case Rep 2016; 17:529-534 :: DOI: 10.12659/AJCR.897572

Keywords: Immunoblastic Lymphadenopathy - therapy, Biopsy, Klinefelter Syndrome - diagnosis, Lymph Nodes - diagnostic imaging, Lymphoma, T-Cell - therapy, Tomography, X-Ray Computed

Published: 2016-07-25, Viewed (1128), Downloaded (9), Related (13), Cited (1)

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Challenging Case of Postmenopausal Bleeding and Complete Urogenital Duplication

Olga Grechukhina, Diana P. English, Devin Miller, Elena Ratner

Am J Case Rep 2016; 17:331-336 :: DOI: 10.12659/AJCR.897080

Keywords: Obesity, Morbid - complications, Postmenopause, Urogenital Abnormalities - diagnosis, Uterine Hemorrhage - etiology

Published: 2016-05-16, Viewed (950), Downloaded (8), Related (6), Cited (1)

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A Case of Beare-Stevenson Syndrome with Unusual Manifestations

Nitin Ron, Samuel Leung, Erin Carney, Alexis Gerber, Karen Laurie David

Am J Case Rep 2016; 17:254-258 :: DOI: 10.12659/AJCR.897177

Keywords: Craniosynostoses - genetics, Acanthosis Nigricans - genetics, Ear - abnormalities, Exons, Infant, Newborn, Mutation, Missense, Natal Teeth, Rare Diseases, Receptor, Fibroblast Growth Factor, Type 2 - genetics, Scalp Dermatoses - genetics, Skin Abnormalities - genetics, Twins, Monozygotic

Published: 2016-04-15, Viewed (1124), Downloaded (23), Related (5), Cited (2)

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Absent Left Main Coronary Artery and Separate Ostia of Left Coronary System in a Patient with Holt-Oram Syndrome and Sinus Node Dysfunction

Thein Tun Aung, Edward Samuel Roberto, Abdul Wase

Am J Case Rep 2016; 17:93-96 :: DOI: 10.12659/AJCR.896474

Keywords: Atrioventricular Block - diagnosis, Abnormalities, Multiple, Coronary Angiography, Coronary Vessel Anomalies - diagnosis, Heart Defects, Congenital - complications, Heart Septal Defects, Atrial - complications, Lower Extremity Deformities, Congenital - complications, Sick Sinus Syndrome - diagnosis, Upper Extremity Deformities, Congenital - complications

Published: 2016-02-17, Viewed (1014), Downloaded (9), Related (9), Cited (1)

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