Congenital Varicella Syndrome - Articles - Scientific Research Publishing

Fatal Neonatal Presentation of Congenital Varicella Syndrome Following First-Trimester Maternal Infection in a Resource Limited Setting: A Case Report (Articles)

Ezioma Anne Alinnor, Chioma Ada Nnah, Nkeiruka Ngozi Iweha, Omoye Winifred Usifo

Open Journal of Pediatrics Vol.16 No.4, July 6, 2026

DOI: 10.4236/ojped.2026.164056 4 Downloads 108 Views Citations
Atypical Presentation of Ramsay Hunt Syndrome without Facial Palsy in an Immunocompetent Senegalese Adulte Patient (Articles)

Daouda Thioub, Aboubakar T. Ibrahim, Khardiata Diallo-Mbaye, Zande-Yindoni Jules, Ndeye A. Lakhe, Moussa Seydi

Case Reports in Clinical Medicine Vol.12 No.7, July 13, 2023

DOI: 10.4236/crcm.2023.127031 240 Downloads 2,887 Views Citations
Anaesthesia for Abscess Drainage in a Six-Month-Old Male with CLOVES Syndrome (Articles)

Onochie Nweze, Ambrose Rukewe, Nala Angula

Open Journal of Anesthesiology Vol.16 No.3, March 12, 2026

DOI: 10.4236/ojanes.2026.163006 76 Downloads 295 Views Citations
Morning Glory Syndrome in Two (02) Malians: Case Report from IOTA-University Hospital (Articles)

Seydou Bakayoko, Brainima Coulibaly, Mohamed Kolé Sidibe, Elien Gyrr, Modibo Sissoko, Gounon Saye, Marcel Tembely, Fatoumata Sylla

Open Journal of Ophthalmology Vol.10 No.3, August 28, 2020

DOI: 10.4236/ojoph.2020.103027 763 Downloads 2,275 Views Citations
Kostmann’s Neutropenia: A Case Report (Articles)

Khaoula Achir, Ilham Tadmori, Mounia Lakhdar Idrissi, Fatima Zahra Souilmi, Mohamed Hbibi, Moustapha Hida

Open Journal of Pediatrics Vol.14 No.5, September 10, 2024

DOI: 10.4236/ojped.2024.145082 114 Downloads 964 Views Citations
Moyamoya Syndrome in Post-Transplant Children with Type 1 Neurofibromatosis and Congenital Nephrotic Syndrome (Articles)

Reyner Loza, Nathalie Rodriguez, Angelica Ynguil, Silvia Sotelo

Open Journal of Nephrology Vol.11 No.4, October 29, 2021

DOI: 10.4236/ojneph.2021.114038 313 Downloads 1,227 Views Citations
The effectiveness and safety of thyroxine replacement therapy for children with down syndrome and subclinical or congenital hypothyroidism—A systematic review (Articles)

Ashwaq H. Al-Sabban, Saleem Ahmed, Jumana Y. Al-Aama

Health Vol.4 No.8, August 29, 2012

DOI: 10.4236/health.2012.48072 4,763 Downloads 7,974 Views Citations
Congenital Nephrotic Syndrome of the Finnish Type: A Greek Case Report (Articles)

Sofia Melina Stasinou, George Valasoulis, Ioannis Georgiou, Kyrgiou Maria, Evangelos Paraskevaidis, Nikolaos Plachouras

Health Vol.6 No.12, June 23, 2014

DOI: 10.4236/health.2014.612176 3,835 Downloads 6,139 Views Citations
Costello Syndrome with Congenital Pulmonary Valve Stenosis and Ventriculomegaly—A Case Report (Case Report)

Ramachandran Muthiah

Case Reports in Clinical Medicine Vol.5 No.8, August 30, 2016

DOI: 10.4236/crcm.2016.58045 2,483 Downloads 5,116 Views Citations
Klippel Trenaunay Syndrome with Angiokeratoma Circumscriptum Naeviforme and Bilateral Congenital Anorchia: A Rare Association (Articles)

Mujammel Haque, Kalyan Benjamin Gomes, Sajib Kumar Talukdhar, Mustafizur Rahman, Farzana Sharmin, Manik Kumar Talukder

Open Journal of Pediatrics Vol.14 No.1, January 8, 2024

DOI: 10.4236/ojped.2024.141005 251 Downloads 1,081 Views Citations
Kiran Nandivada’s Stuck Blade in a Grinder Jar Degenerative Cascade by LSTV at L5-S1 (Articles)

Venkata Satya Kumar Kiran Nandivada, Nadavinamani Shivanand Raghavendra, Nandivada Nikhil Bharadwaja, Moola Sohith Mahadeva Reddy, Ahmed Usama Rizvi

Open Journal of Orthopedics Vol.14 No.1, January 16, 2024

DOI: 10.4236/ojo.2024.141002 253 Downloads 915 Views Citations
Sirenomelie (Mermaid Syndrome): A Case Report and Literature Review (Articles)

Faya Daniel Sewadouno, Christel Lalèyè, Simon Azonbakin, Morel Koutangni, Younoussa Kourouma, Fara Yangba Kamano, Tamba Elie Tolno

Open Journal of Pathology Vol.16 No.1, November 18, 2025

DOI: 10.4236/ojpathology.2026.161003 83 Downloads 568 Views Citations
Slow and Steady: The Cautious Use of Neuroleptics in a Patient with Andersen-Tawil Syndrome (Articles)

Fahad Alkhalfan, Bharadwaj Adithya-Sateesh, Girma M. Ayele, Merve Otles, Rediet T. Atalay, Miriam Michael

Case Reports in Clinical Medicine Vol.11 No.10, October 9, 2022

DOI: 10.4236/crcm.2022.1110058 206 Downloads 1,026 Views Citations
Moebius-Poland Syndrome: A Case Report from West Africa (Articles)

Warigbani Pieterson, Richfield Akpaka, Emmanuel Jackson, Elleisabeth Pieterson, Simpson Mensah

Modern Plastic Surgery Vol.15 No.4, September 29, 2025

DOI: 10.4236/mps.2025.154010 98 Downloads 456 Views Citations
A Case Report: PCR-Assisted Diagnosis of Varicella in an Adult (Articles)

Satish K. Mehta, Don Gilden, Brian E. Crucian, Clarence F. Sams, Randall J. Cohrs, Duane L. Pierson

Open Journal of Medical Microbiology Vol.2 No.3, September 26, 2012

DOI: 10.4236/ojmm.2012.23019 3,994 Downloads 6,791 Views Citations
Non genetic risk factors of long-QT syndrome (Articles)

Ewa Moric-Janiszewska, Grzegorz Hibner

Open Journal of Genetics Vol.2 No.1, March 2, 2012

DOI: 10.4236/ojgen.2012.21007 5,941 Downloads 10,341 Views Citations
MDCT Angiography Imaging Presentation of ALCAPA in Adults (Articles)

Qinyi Dai, Biao Lv, Zhaoqi Zhang

Advances in Computed Tomography Vol.2 No.1, March 8, 2013

DOI: 10.4236/act.2013.21005 5,038 Downloads 9,548 Views Citations
Does DKC1 Mutation Suffice to Define the Phenotype Severity of Hoyeraal-Hreidarsson Syndrome? (Articles)

Elvis Terci Valera, María Sol Brassesco, Sabrine Teixeira Ferraz, Pérsio Roxo Jr., Barbara Lemos-Santana, Tom Vulliamy, Rodrigo Tocantins Calado, Carlos Alberto Scrideli, Luiz Gonzaga Tone

Open Journal of Blood Diseases Vol.3 No.1, March 29, 2013

DOI: 10.4236/ojbd.2013.31012 3,929 Downloads 6,781 Views Citations
Apert Syndrome: A Case Report and Review of Literature (Articles)

Simon Pius, Halima Abubakar Ibrahim, Mustapha Bello, Kefas Mbaya, Jose Pwavimbo Ambe

Open Journal of Pediatrics Vol.6 No.2, June 9, 2016

DOI: 10.4236/ojped.2016.62026 3,103 Downloads 7,378 Views Citations
Multiple Major Thrombo-Embolic Events, including Stroke, in a Patient with Combined Congenital Anti-Thrombin III Deficiency and MTHFR Homozygous Mutation (Articles)

Islam I. Zaid, Nora I. Abbas, Ehab Shaker, Foad Abd-Allah

World Journal of Cardiovascular Diseases Vol.7 No.3, March 27, 2017

DOI: 10.4236/wjcd.2017.73008 1,589 Downloads 2,931 Views Citations

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