نتائج البحث

Glucose-6-phosphate dehydrogenase deficiency as a cause for nonimmune hydrops fetalis and severe fetal anemia: A systematic review.

• Authors : Iyer NS; Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.; Mossayebi MH

Subjects: Hydrops Fetalis*/Hydrops Fetalis*/Hydrops Fetalis*/etiology ; Hydrops Fetalis*/Hydrops Fetalis*/Hydrops Fetalis*/diagnosis ; Glucosephosphate Dehydrogenase Deficiency*/Glucosephosphate Dehydrogenase Deficiency*/Glucosephosphate Dehydrogenase Deficiency*/complications

• Source: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Jul; Vol. 12 (7), pp. e2491.Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print Cited Medium: Internet ISSN:

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Fetal Anemia and Hydrops Fetalis Associated with Homozygous Hb Constant Spring (HBA2: c.427T > C).

• Authors : He Y; a Prenatal Diagnostic Center, Dongguan Maternal & Children Health Hospital , Dongguan, Guangdong , People's Republic of China and.; Zhao Y

Subjects: Homozygote* ; Mutation*; Anemia/Anemia/Anemia/*genetics

• Source: Hemoglobin [Hemoglobin] 2016; Vol. 40 (2), pp. 97-101. Date of Electronic Publication: 2016 Jan 13.Publisher: Informa Healthcare Country of Publication: England NLM ID: 7705865 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Glucose-6-Phosphate Dehydrogenase Deficiency as a Cause for Nonimmune Hydrops Fetalis and Severe Fetal Anemia: A Systematic Review

• Authors : Iyer, Neel S.; Mossayebi, Matthew H.; Gao, Tracy J.

Subjects: fetal anemia; G6PD deficiency; hydrops fetalis

• Source: Department of Obstetrics and Gynecology Faculty Papers

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Glucose phosphate isomerase (GPI) Tadikonda: Characterization of a novel Pro340Ser mutation.

• Authors : Zaidi AU; a Divison of Pediatric Hematology , Children's Hospital of Michigan, Wayne State University School of Medicine , Detroit , MI , USA.; Kedar P

Subjects: Homozygote* ; Mutation, Missense*; Anemia/Anemia/Anemia/*genetics

• Source: Pediatric hematology and oncology [Pediatr Hematol Oncol] 2017 Nov; Vol. 34 (8), pp. 449-454. Date of Electronic Publication: 2017 Dec 11.Publisher: Informa Healthcare Country of Publication: England NLM ID: 8700164 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Perinatal Lethal Gaucher Disease due to RecNcil Recombinant Mutation in the GBA Gene Presenting with Hydrops Fetalis and Severe Congenital Anemia.

• Authors : Bhutada, Ekta^1,2; Pyragius, Timothy³; Petersen, Scott G.⁴

• Source: Case Reports in Pathology. 5/9/2018, p1-4. 4p.

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Fetal-onset congenital dyserythropoietic anemia type 1 due to CDAN1 mutations presenting as hydrops fetalis.

• Authors : Liu, Sha¹; Liu, Ying-Na²; Zhen, Li³

• Source: Pediatric Hematology & Oncology. Oct/Nov2018, Vol. 35 Issue 7/8, p447-450. 4p.

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Short Neonatal Outcomes after Intrauterine Transfusion in Fetal Anemia, the Experience from a Referral Academic Center.

• Authors : Shirazi, Mahboobeh¹; Feizabad, Elham²; Bahmanpour, Ghazaleh¹

• Source: Iranian Journal of Neonatology. Oct2022, Vol. 13 Issue 4, p28-33. 6p.

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Hydrops Fetalis due to Kell Alloimmunization: A Perinatal Approach to a Rare Case.

• Authors : Akdağ, Arzu¹ ; Erdeve, Ömer¹; Uraş, Nurdan¹

• Source: Turkish Journal of Hematology. Mar2012, Vol. 29 Issue 1, p72-75. 4p.

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Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias.

• Authors : Shefer Averbuch N; Schneider Children's Medical Center of Israel, Petach Tikva, Israel.; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Subjects: Genetic Association Studies*; Anemia/Anemia/Anemia/*congenital ; Anemia/Anemia/Anemia/*diagnosisPyruvate Kinase Deficiency of Red Cells; Xerocytosis, hereditary

• Source: European journal of haematology [Eur J Haematol] 2018 Sep; Vol. 101 (3), pp. 297-304. Date of Electronic Publication: 2018 Jun 25.Publisher: Blackwell Country of Publication: England NLM ID: 8703985 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1600-0609

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Diagnostic value of fetal hemoglobin Bart's for evaluation of fetal α-thalassemia syndromes: application to prenatal characterization of fetal anemia caused by undiagnosed α-hemoglobinopathy.

• Authors : Singha, Kritsada^1,2 (AUTHOR); Yamsri, Supawadee¹ (AUTHOR); Chaibunruang, Attawut¹ (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 2/10/2022, Vol. 17 Issue 1, p1-9. 9p.

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