Cargando…
Idiopathic Pulmonary Hemosiderosis Mimicking Iron Deficiency Anemia: A Delayed Diagnosis?
Idiopathic pulmonary hemosiderosis (IPH) is an uncommon chronic disorder in children. It is characterized by recurrent pulmonary hemorrhage and may result in hemoptysis and pulmonary insufficiency. The most common hematologic manifestation of IPH is iron deficiency anemia. The etiology of IPH is not...
Autores principales: | Koker, Sultan Aydin, Gözmen, Salih, Oymak, Yeşim, Karapinar, Tuba Hilkay, Can, Demet, Genç, Sinan, Vergin, Raziye Canan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PAGEPress Publications, Pavia, Italy
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5477471/ https://www.ncbi.nlm.nih.gov/pubmed/28670434 http://dx.doi.org/10.4081/hr.2017.7048 |
Ejemplares similares
-
Thrombotic Microangiopathy with Complement Factor H Gene Mutations Unassociated with Atypical Hemolytic Uremic Syndrome
por: Oymak, Yeşim, et al.
Publicado: (2015) -
262. Assessment of Serum Galactomannan Test Results of Pediatric Patients with Hematologic Malignancies According to Different Threshold Levels and Consecutive Positivity in Terms of Invasive Aspergillosis Diagnosis: Cross-Sectional Research in a Tertiary Care Hospital
por: Çağlar, İlknur, et al.
Publicado: (2019) -
Late diagnosis of leukocyte adhesion deficiency type II and Bombay blood type in a child: a rare case report
por: Yaman, Yöntem, et al.
Publicado: (2019) -
Idiopathic Pulmonary Hemosiderosis: The Great Hemolytic Anemia Mimicker
por: Chan, Jaclyn
Publicado: (2023) -
A Neonatal Case of Infantile Malignant Osteopetrosis Presenting with Thrombocytopenia and Hypotonicity: A Novel Mutation in Chloride Voltage-Gated Channel 7 Gene
por: Odaman Al, Isik, et al.
Publicado: (2022)