Results 81 to 90 of about 8,139 (212)
Anaemia is not a diagnosis: Part 2
South African Family Practice, 1987 No abstract available.
D.G. Kenoyer
doaj +1 more source
What's Your Diagnosis? A Case of Extreme Thrombocytosis in a Dog
Veterinary Clinical Pathology, EarlyView.
Stephanie F. Anderson +5 more
wiley +1 more source
Severe Lactic Acidosis in Decompensated Cirrhosis Despite Nondiagnostic Imaging
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Lactic acidosis is a strong predictor of mortality in cirrhosis, reflecting both impaired hepatic clearance and systemic tissue hypoxia. We describe a 38‐year‐old man with decompensated alcohol‐associated cirrhosis who developed severe lactic acidosis despite stable hemodynamics and initially nondiagnostic vascular imaging.
Nakul Ganju +5 more
wiley +1 more source
, 2020 This study aimed to assess significance in complete blood counts and biochemical markers in the diagnosis of macrocytic anemias. To achieve the goal, the following tasks were set: to assess the frequency of macrocytic anemias and their relationship to ...
Barčaitė, Irma
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Indian Dermatology Online Journal, 2014 Rud′s syndrome is a rare autosomal recessive hereditary disorder characterized by congenital ichthyosis, epilepsy, dwarfism, sexual infantilism, polyneuritis, and macrocytic anemia.
K Pavani, B. S. N. Reddy, B Amar Singh
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT This case report describes a 77‐year‐old man with multiple comorbidities, including atrial fibrillation, heart failure with mildly reduced ejection fraction, hypertension, diabetes mellitus, and prior coronary artery bypass grafting, who presented with severe hypertension and dyspnoea.
Reem Fakak +2 more
wiley +1 more source
Isolated Palmar Hyperpigmentation: Rare Presentation of B12 Deficiency
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Vitamin B12 deficiency has a myriad of presentations. Skin hyperpigmentation, especially at the knuckles, is common. However, in rare instances, a patient may present with isolated palmar hyperpigmentation instead of the usual features, such as knuckle hyperpigmentation, smooth tongue, symptoms related to anemia, and neurologic features.
Mukti Nath Sankhi +4 more
wiley +1 more source
Sanjad-Sakati syndrome with macrocytic anemia and failure to thrive: a case from South Jordan
, 2018 Backgorund: Sanjad-Sakati syndrome (SSS) is a rare autosomal recessive disease caused by a deletion mutation (155–166del) in exon 3 of the TBCE gene on chromosome 1q42-43.
Salma A. Ajarmeh, Eyad M. Al Tamimi
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, 2021 During red blood cell (RBC) lysis hemoglobin and heme leak out of the cells and cause damage to the endothelium and nearby tissue. Protective mechanisms exist; however, these systems are not sufficient in diseases with increased extravascular hemolysis e.
Bergwik, Jesper, +10 more
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