Results 71 to 80 of about 7,512,016 (281)

Fecal microbiota transplantation and microbiota‐based therapeutics in pediatric clinical practice: Current status and emerging indications

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Fecal microbiota transplantation (FMT) is a safe and effective treatment for recurrent or refractory Clostridioides difficile infection (rCDI) in children and adults. This review outlines the evidence behind FMT for rCDI, considerations in special pediatric populations, and limitations in current practice due to FMT access for patients under ...
Nikhil Pai, Maribeth Nicholson, Steven Rich, Máire A. Conrad   +3 more
wiley   +1 more source

Unusual Presentation of Brain Aspergillosis in Chronic Granulomatous Disease

, 2010
Aspergillus is a frequently observed pathogen in patients with chronic granulomatous disease. We report on a patient with chronic granulomatous disease and severe brain aspergillosis with an unusual presentation and favorable course.
Ullissis Pádua de Menezes, TAKAYANAGUI, Osvaldo M., CONDINO-NETO, Antonio, Pérsio Roxo, FERRIANI, Virginia Paes Leme, MENEZES, Ullissis Padua de, Antônio Condino-Neto, ROXO JR., Persio, Virgínia Paes Leme Ferriani, Osvaldo M. Takayanagui   +9 more
core   +1 more source

A hepatic enigma: Pediatric presentation of primary biliary cholangitis

JPGN Reports, EarlyView.
Abstract Primary biliary cholangitis (PBC) is a chronic autoimmune condition characterized by destruction of intrahepatic bile ducts, leading to fibrosis and cirrhosis of the liver. It is an extremely rare pediatric disease with very few pediatric cases reported to date. Here, we report the case of a 14‐year‐old female who presented with elevated liver
Sindhura Kasturi, Rachel Schenker, Nick Shillingford, George Yanni   +3 more
wiley   +1 more source

Chronic Granulomatous Disease Associated with Chronic Glomerulonephritis

, 1985
A boy with chronic granulomatous disease (CGD) developed glomerulonephritis at the age of 12 years. The glomerulonephritis progressed to terminal uraemia at age 15 when maintenance haemodialysis was started.
J. J. FRIFELT, N. H. VALERIUS, H. STARKLINT, M. STRATE, Schønheyder, Henrik Carl, H. SCHØNHEYDER, Valerius, Niels Henrik, Strate, M, Starklint, H, Frifelt, J J   +9 more
core   +1 more source

Human immunodeficiency virus infection mimicking very early onset inflammatory bowel disease

JPGN Reports, EarlyView.
Abstract Very early onset inflammatory bowel disease (VEO‐IBD), defined as diagnosis before 6 years of age, is often associated with immune dysregulation and monogenic etiologies; however, infectious mimics may be overlooked in low‐prevalence regions. We report a 4‐year‐old male with poor weight gain, intermittent diarrhea, elevated fecal calprotectin,
Rasha Abi Radi Abou Jaoudeh, Cary Sauer, Teresa Oh   +2 more
wiley   +1 more source

Vedolizumab use for severe chronic enterocolitis in a child with Hoyeraal–Hreidarsson syndrome: A case report

JPGN Reports, EarlyView.
Abstract We report a patient with Hoyeraal–Hreidarsson syndrome (HHS), a telomere biology disorder, who developed severe chronic enterocolitis with inflammatory bowel disease‐like features. Vedolizumab led to improvement in stool frequency, reduced fecal calprotectin, and clinical remission without infectious complications.
Yasutaka Chiba, Manabu Takahashi, Taro Yoshida, Seiya Tagane, Takeshi Shiohata, Shoko Miura, Manami Akasaka   +6 more
wiley   +1 more source

Refractory Eczema as a Presenting Feature of Common Variable Immunodeficiency

JEADV Clinical Practice, EarlyView.
ABSTRACT Common variable immunodeficiency (CVID) is the most prevalent symptomatic inborn error of immunity (IEI) in adults. It presents with recurrent infections and non‐infectious complications, including autoimmunity, lymphoproliferation and dermatitis.
Mercedes Sanchez‐Diaz, Lars Matthies, Andrea Vanegas Ramirez   +2 more
wiley   +1 more source

Salmonella Enteritidis cholecystitis with chronic granulomatous disease

IDCases, 2018
We describe a 40-year-old woman with Salmonella cholecystitis complicating adult-onset X-linked chronic granulomatous disease (CGD) caused by a de novo mutation in the paternal-origin CYBB gene.
Yuki Yamashita, Takefumi Kimura, Naoki Tanaka, Masahide Yazaki, Tadashi Itagaki, Satoru Joshita, Takeji Umemura, Akihiro Matsumoto, Hiromitsu Mori, Shuichi Wada, Eiji Tanaka   +10 more
doaj   +1 more source

Case Reports A case of chronic granulomatous disease

, 2014
(Key words: Chronic granulomatous disease; phagocyte ...
S Sriranganathan, G N Lucas, S Gunawardene, N R De Silva   +3 more
core  

Pulmonary Aspergillosis in a Previously Healthy 13-Year-Old Boy

Canadian Respiratory Journal, 2016
Chronic granulomatous disease (CGD) is a rare, polygenic primary immunodeficiency. In this case report, we describe a previously healthy 13-year-old boy who presented with multifocal pulmonary aspergillosis and was subsequently diagnosed with an ...
Jonathan H. Rayment, Indra Narang
doaj   +1 more source