Results 61 to 70 of about 1,674 (114)

Cyanosis by methemoglobinemia in tadpoles of Cochranella granulosa (Anura: Centrolenidae)

Revista de Biología Tropical, 2010
Tadpoles inhabit generally well oxygenated rivers and streams, nevertheless they were found in areas with limited oxygen availability inside the rivers.
Heinz Hoffmann
doaj  

Long QT Syndrome Type 5 With Coexisting KCNE1 and RYR2 Variants: A Diagnostic Ambiguity

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Long QT syndrome (LQTS) predisposes to syncope and sudden cardiac death. Type 5 LQTS, linked to KCNE1 variants, is rare. A teenage female presented with recurrent syncope. ECG showed QTc 485 ms. Genetic testing identified KCNE1 and RYR2 variants. Beta‐blockers and ICD prevented events.
Mohammad Hossein Nikoo, Hossein Fatemian, Amir Hossein Hassani, Mehrdad Rabiee Rad, Sara Mostafavi   +4 more
wiley   +1 more source

Palliative Right Ventricular Outflow Tract Stenting in Tetralogy of Fallot with Severe Cyanosis: Experience from a Single Center in Southern India

Current Medical Issues
Background: This study conducted at an Indian tertiary care hospital aimed to characterize the clinical profile of tetralogy of Fallot (ToF) patients undergoing right ventricular outflow tract (RVOT) stenting and assess their immediate postprocedural ...
Bhavana Priyadarshini, Sowmya Kasturi, Srinath N. Reddy, Satish Mohanty   +3 more
doaj   +1 more source

Diagnostic and Therapeutic Challenges in Statin‐Induced Necrotizing Autoimmune Myopathy in an Elderly Patient: A Rare Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT We present the case of a 78‐year‐old woman with metabolic syndrome and a history of multiple ischemic strokes who developed progressive symmetrical proximal muscle weakness, predominantly affecting the lower extremities, while on atorvastatin.
Nischal Shrestha, Abdirahman Hassan, Jennifer Ann Evans   +2 more
wiley   +1 more source

A needle in a haystack: Navigating equine injectable drug reactions

Equine Veterinary Education, EarlyView.
G. D. Hallowell
wiley   +1 more source

Co‐infection of Hepatitis A and E With Atypical Manifestation: A Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Hepatitis A virus (HAV) and hepatitis E virus (HEV) are common causes of acute viral hepatitis in developing countries where inadequate sanitation and contaminated water supplies facilitate fecal–oral transmission. Although both infections are usually self‐limiting, co‐infection may result in atypical presentations and pose diagnostic ...
Umaimah Batool Mirza, Habib Ul Rahman Kalhoro, FNU Umna, Ahmed Asad Raza, Abedin Samadi   +4 more
wiley   +1 more source

Loss of Consciousness in a Child Following Accidental Ingestion of Brimonidine Ointment: A Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Brimonidine ingestion in young children can cause rapid, severe central nervous system (CNS) depression, including miosis and hypotonia. Clinicians should maintain a high index of suspicion in toddlers presenting with unexplained drowsiness following exposure.
Ramin Zare Mahmoudabadi, Maryam Vafapour, Majid Karubi, Zahra Noori Etemad, Mohammad Mohammadi, Seyed Reza Gholizadeh, Aynaz Mohammadi   +6 more
wiley   +1 more source

Peritoneopericardial hernioplasty in a two-month-old Shih Tzu

Open Veterinary Journal
Background: Peritoneopericardial hernias (PPHs) are defects of ccontnuity between the diaphragm and the peritoneum that allow the transposition of abdominal organs into the thoracic cavity, which can lead to clinical, gastroenterological, and ...
Rafaela Rodrigues Ribeiro, Guilherme Pinheiro Santos, Marco Augusto Machado Silva, Cindy Stefhani dos Santos Silva, Tayanne Gobbi Mendes, Rauane Sousa de Moura, Iago Martins Oliveira   +6 more
doaj   +1 more source

Cat Eye Syndrome in a Sudanese Infant: Congenital Cataract in the Absence of Iris Coloboma: A Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT We report the first Cat Eye Syndrome case from Sudan: a 5‐month‐old female with growth retardation, craniofacial dysmorphism, congenital cataract without iris coloboma, and ventricular septal defect. Cytogenetics confirmed 47,XX,+idic(22)(q11.2).
Rayan Khalid, Imad Fadl‐Elmula
wiley   +1 more source

METHEMOGLOBINEMIA WITH NEUROLOGICAL MANIFESTATIONS: A CASE OF RECESSIVE CONGENITAL METHEMOGLOBINEMIA TYPE II

İstanbul Tıp Fakültesi Dergisi
Congenital methemoglobinemia is a rare cause of cyanosis that is characterized by increased methemoglobin levels and caused by mutations in the cytochrome B5 reductase 3 (CYB5R3) gene resulting in deficiencies of the nicotinamide adenine dinucleotide ...
Müjgan Arslan, Kübra Boztepe, Veysel Atilla Ayyıldız, Halil Özbaş   +3 more
doaj   +1 more source