Nonimmune hydrops fetalis in two cases of consanguineous parents and associated with hereditary spherocytosis and hemophagocytic hystiocytosis
Nonimmune hydrops fetalis may occur as a result of different etiological conditions and in about one-third of cases no cause could be identified. Here, we report two cases of nonimmune hydrops fetalis associated with hereditary spherocytosis and hemophagocytic hystiocytosis. We think that babies wit...
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| Published in | Journal of Perinatology Vol. 27; no. 4; pp. 252 - 254 |
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| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
| Published |
United States
Nature Publishing Group
01.04.2007
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| Abstract | Nonimmune hydrops fetalis may occur as a result of different etiological conditions and in about one-third of cases no cause could be identified. Here, we report two cases of nonimmune hydrops fetalis associated with hereditary spherocytosis and hemophagocytic hystiocytosis. We think that babies with hydrops fetalis born of consanguineous parents should be examined for hereditary diseases, and that these rare causes should be taken into account in problematic cases. |
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| AbstractList | Nonimmune hydrops fetalis may occur as a result of different etiological conditions and in about one-third of cases no cause could be identified. Here, we report two cases of nonimmune hydrops fetalis associated with hereditary spherocytosis and hemophagocytic hystiocytosis. We think that babies with hydrops fetalis born of consanguineous parents should be examined for hereditary diseases, and that these rare causes should be taken into account in problematic cases. |
| Audience | Academic |
| Author | Gurakan, F Yetgin, S Aytac, S Yurdakok, M |
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/17377610$$D View this record in MEDLINE/PubMed |
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| Cites_doi | 10.1016/S0146-0005(05)80052-7 10.1182/asheducation-2005.1.13 10.1007/s004310051314 10.1111/j.1365-2141.1991.tb04429.x 10.1182/blood.V78.11.3043.3043 10.1016/S0002-9378(86)80026-6 10.1016/j.critrevonc.2004.11.002 10.1172/JCI119155 10.1016/S0889-8588(05)70521-9 10.1046/j.1365-2141.2003.04726.x 10.1111/j.1365-2141.1999.01130.x 10.1172/JCI117766 10.1038/sj.jp.7211121 10.1182/blood-2001-12-0351 10.1172/JCI119041 |
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| References_xml | – volume: 124 start-page: 4 year: 2004 end-page: 14 article-title: Modern management of children with hemophagocytic lymphohistiocytosis publication-title: Br J Haematol contributor: fullname: Schneider, EM – volume: 155 start-page: 812 year: 1986 end-page: 816 article-title: Nonimmune hydrops fetalis: clinical experience and factors related to a poor outcome publication-title: Am J Obstet Gynecol contributor: fullname: Geist, D – volume: 159 start-page: 481 year: 2000 end-page: 492 article-title: Hydrops fetalis associated with erythrocyte pyruvate kinase deficiency publication-title: Eur J Pediatr contributor: fullname: Araujo, F – volume: 19 start-page: 447 year: 1995 end-page: 461 article-title: Non immune fetal hydrops: diagnosis and obstetrical management publication-title: Semin Perinatol contributor: fullname: Jones, DC – volume: 98 start-page: 2300 year: 1996 end-page: 2307 article-title: Combination of two mutant spectrin alleles underlies severe spherocytic hemolytic anemia publication-title: J Clin Invest contributor: fullname: Jarolim, P – volume: 95 start-page: 1174 year: 1995 end-page: 1182 article-title: Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene publication-title: J Clin Invest contributor: fullname: Marchesi, SL – volume: 78 start-page: 3043 year: 1991 end-page: 3051 article-title: Deficiency of -spectrin synthesis in burst forming units - erythroid in lethal hereditary spherocytosis publication-title: Blood contributor: fullname: Miller, BA – start-page: 13 year: 2005 end-page: 18 article-title: Red cell membrane disorders publication-title: American Society of Hematology 47th Annual Meeting Educating Program Book contributor: fullname: Bonkovky, HL – volume: 78 start-page: 278 year: 1991 end-page: 280 article-title: Sea blue histiocytes in the bone marrow of variant chronic granulomatous disease with residual monocyte NADPH-oxidase activity publication-title: Br J Haematol contributor: fullname: Heyne, K – volume: 12 start-page: 435 year: 1998 end-page: 444 article-title: Infection and malignancy-associated hemophagocytic syndromes: secondary hemophagocytic lymphohistiocytosis publication-title: Hematol Oncol Clin North Am contributor: fullname: Henter, J-I – volume: 100 start-page: 356 year: 2002 end-page: 358 article-title: Hydrops fetalis-associated congenital dyserythropoietic anemia treated with intrauterine transfusions and bone marrow transplantation publication-title: Blood contributor: fullname: Ginovart, G – volume: 99 start-page: 267 year: 1997 end-page: 277 article-title: Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia publication-title: J Clin Invest contributor: fullname: Mohandas, N – volume: 104 start-page: 2 year: 1999 end-page: 13 article-title: Red blood cell membrane disorders publication-title: Br J Haematol contributor: fullname: Lux, SE – volume: 3 start-page: 85 year: 2004 end-page: 91 article-title: Update on the clinical spectrum and genetics of red blood cell membrane disorders publication-title: Curr Hematol Rep contributor: fullname: Gallagher, PG – volume: 24 start-page: 458 year: 2004 end-page: 460 article-title: Hemophagocytic lymphohistiocytosis presenting with nonimmune hydrops fetalis publication-title: J Perinatol contributor: fullname: Challapalli, M – volume: 18 start-page: 29 year: 1991 end-page: 33 article-title: Diagnostic guidelines for hemophagocytic lymphohistiocytosis. 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| Snippet | Nonimmune hydrops fetalis may occur as a result of different etiological conditions and in about one-third of cases no cause could be identified. Here, we... |
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| SubjectTerms | Cancer Care and treatment Case studies Chemotherapy Consanguinity Diagnosis Diseases Edema Etiology Fatal Outcome Female Health aspects Hereditary diseases Hereditary spherocytosis Humans Hydrops fetalis Hydrops Fetalis - etiology Infant, Newborn Infants (Newborn) Lymphohistiocytosis, Hemophagocytic - complications Male Patient outcomes Risk factors Spherocytosis Spherocytosis, Hereditary - complications |
| Title | Nonimmune hydrops fetalis in two cases of consanguineous parents and associated with hereditary spherocytosis and hemophagocytic hystiocytosis |
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