Recurrent sideroblastic anemia during pregnancy

Autor: Shehab Mohamed, Firyal Ibrahim, Mohamad Najib Alasafar, Awni Alshurafa, Susanna Akiki, Dina Soliman, Samah Kohla, Aliaa Amer, Hana Qasim, Honar Cherif

Publikováno v: Clinical Case Reports, Vol 11, Iss 1, Pp n/a-n/a (2023)

Abstract Sideroblastic anemia is a heterogeneous group of disorders typified by the presence of ring sideroblasts in the bone marrow and has congenital and acquired types. Sideroblastic anemia is a rare event in pregnancy. We report a case of a 32‐

Externí odkaz: https://doaj.org/article/d76762a52f3e4acbad9d2a4bbb11f201

Wilson's Disease in Children: A Position Paper by the Hepatology Committee of the European Society for Paediatric Gastroenterology, Hepatology and Nutrition

Autor: Roderick H. J. Houwen, Dominique Debray, Jörg Jahnel, Nedim Hadzic, Françoise Smets, Wojciech Jańczyk, Loreto Hierro, Lorenzo D'Antiga, Stuart Tanner, Valerio Nobili, Raffaele Iorio, Ulrich Baumann, Anil Dhawan, Björn Fischler, Antal Dezsofi, Piotr Socha, Henkjan J. Verkade, Pietro Vajro, Valérie A. McLin

Publikováno v: Journal of Pediatric Gastroenterology and Nutrition, 66(2), 334-344. Lippincott Williams and Wilkins
Journal of Pediatric Gastroenterology and Nutrition, 66(2), 334. Lippincott Williams and Wilkins

Background:Clinical presentations of Wilson's disease (WD) in childhood ranges from asymptomatic liver disease to cirrhosis or acute liver failure, whereas neurological and psychiatric symptoms are rare. The basic diagnostic approach includes serum c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eac67ce95ad0acb0bc6e6944b2944631
https://research.rug.nl/en/publications/1d6bf2d7-ad7c-4c17-8f9c-c388c42c3658

Iron metabolism in erythroid cells and patients with congenital sideroblastic anemia

Autor: Kiriko Kaneko, Kazumichi Furuyama

Publikováno v: International journal of hematology. 107(1)

Sideroblastic anemias are anemic disorders characterized by the presence of ring sideroblasts in a patient's bone marrow. These disorders are typically divided into two types, congenital or acquired sideroblastic anemia. Recently, several genes were

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::975198bff25a141f7414c6ba9a103691
https://pubmed.ncbi.nlm.nih.gov/29139060

Ringed sideroblasts in β-thalassemia

Autor: Amy E. Caruso Brown, Dean R. Campagna, Hassan M. Yaish, Klaus Schmitz-Abe, Mark D. Fleming, Kyriacos Markianos, Kim Cattivelli, Susan Kearney, Ellis J. Neufeld, Matthew M. Heeney, Kelly Walkovich

Publikováno v: Pediatric Blood & Cancer. 64:e26324

Symptomatic β-thalassemia is one of the globally most common inherited disorders. The initial clinical presentation is variable. Although common hematological analyses are typically sufficient to diagnose the disease, sometimes the diagnosis can be

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d26b0b148aa871f9e83569745723fa8d
https://doi.org/10.1002/pbc.26324

Recurrent acquired sideroblastic anemia in a twin pregnancy

Autor: Christopher W.G. Redman, Lawrence Impey, Catherine Greenwood, Adrian Taylor, J. S. Wainscoat

Publikováno v: The Journal of Maternal-Fetal Medicine. 9:248-249

A woman whose sideroblastic anemia had relapsed with progestogen and combined oral contraceptive therapy suffered further relapses in a (twin) pregnancy. Previous reports exist of relapses both from progestogens and in pregnancy, and we postulate a s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e37eb442d5ac4b833ce3d911ec4b75d
https://doi.org/10.1002/1520-6661(200007/08)9:4<248::aid-mfm12>3.0.co