Successful elimination of factor VIII inhibitor using cyclosporin A [PDF]
, 2003 No abstract ...
Dykes +10 more
core +1 more source
Clinical Case Reports, Volume 14, Issue 4, April 2026.ABSTRACT Isoimmunization and fetal anemia pose considerable challenges in obstetrics, especially when there is a documented history of RhD incompatibility or other antibodies that may threaten fetal well‐being. These conditions frequently result in serious complications, including hydrops fetalis, fetal anemia, and, in certain situations, fetal loss ...
Fatemeh Golshahi +8 more
wiley +1 more source
Recém-nascido com hidrópsia fetal não imune - experiência de um centro de referência.
Acta Médica Portuguesa, 2008 Nonimmune hydrops fetalis is a rare affection that can result from several disorders. Notwithstanding with the advances in the diagnosis and treatment, its morbidity and mortality are still very high.
Ana Teixeira +3 more
doaj +1 more source
Long-Term Follow-up Posthematopoietic Stem Cell Transplantation in a Japanese Patient with Type-VII Mucopolysaccharidosis [PDF]
, 2020 The effectiveness of hematopoietic stem cell transplantation (HSCT) for type-VII mucopolysaccharidosis (MPS VII, Sly syndrome) remains controversial, although recent studies have shown that it has a clinical impact. In 1998, Yamada et al.
Fukao, Toshiyuki +4 more
core +1 more source
Clinical Case Reports, Volume 14, Issue 4, April 2026.ABSTRACT The cartilage hair hypoplasia‐anauxetic dysplasia (CHH‐AD) spectrum represents a group of rare autosomal recessive skeletal dysplasias with significant phenotypic heterogeneity. These disorders are classified based on pathogenic variants in the RMRP, POP1, and NEPRO genes.
Mahnaz Mohammadi Kian +6 more
wiley +1 more source
Case report: Giant congenital pulmonary airway malformation initially managed and resected on ECMO
Journal of Pediatric Surgery Case Reports, 2016 Congenital pulmonary airway malformations (CPAM) are a common congenital anomaly, occurring as a result of aberrant formation of pulmonary lobes or segments. Many patients with CPAM are treated with postnatal surgical excision within 1-year of age.
Richard Yeker +3 more
doaj +1 more source
Increased incidence of cytogenetic abnormalities in chorionic villus samples from pregnancies established by in vitro fertilization and embryo transfer (IVF-ET) [PDF]
, 1995 We studied 201 pregnancies that were established by in vitro fertilization and embryo transfer (IVF–ET) and compared the frequency of cytogenetic abnormalities with that found in a large control population matched for indication group (advanced maternal ...
Berg, C.D.F. (Cardi) van den +8 more
core +1 more source
Comparison of the HbH inclusion test and a PCR test in routine screening for α thalassaemia in Hong Kong [PDF]
, 1996 Aim - To compare the haemoglobin (Hb) H inclusion test with a polymerase chain reaction CPCR) test in routine screening for or thalassaemia. Methods - Ninety nine peripheral blood samples from Chinese patients with mean corpuscular volume below 80fl were
Chan, AYY, Chan, LC, So, CKC
core
Analysis of Non-Immune Hyrops Fetalis: Evaluation of 15 Cases
Gynecology Obstetrics & Reproductive Medicine, 2012 OBJECTIVES: To evaluation the ultrasound characteristics, etiological factors and perinatal outcome in hydrops fetalis. STUDY DESIGN: A total of 15 hydrops fetalis presented in our perinatology unit, were studied prospectively.
Turhan Aran +2 more
doaj
Kasabach-Merritt phenomenon and prenatal counseling: a case series. [PDF]
, 2016 Kasabach-Merritt phenomenon can be encountered in the perinatal period. No consensus exists regarding prenatal management. We report one prenatal case leading to therapeutic abortion and one neonatal case, successfully treated by a multimodal therapy ...
Beissel, A. +6 more
core +1 more source