1.Twelve cases of nonimmune hydrops fetalis.
Sung Won YANG ; Yun Sil CHANG ; Hee Seop KIM ; Young Pyo CHANG ; Beyong Il KIM ; Jung Hwhan CHOI ; Chong Ku YUN
Korean Journal of Perinatology 1993;4(4):588-593
No abstract available.
Hydrops Fetalis*
2.A clinical study on nonimmune hydrops fetalis.
Yong Seok JEE ; Sei Kwang KIM ; Young Ho YANG ; Chan Ho SONG
Korean Journal of Obstetrics and Gynecology 1993;36(7):1793-1799
No abstract available.
Hydrops Fetalis*
3.A case of nonimmune hydrops fetalis.
Kwang Soon PARK ; Yong CHO ; Yong Phil KIM
Korean Journal of Obstetrics and Gynecology 1993;36(6):869-876
No abstract available.
Hydrops Fetalis*
4.Clinical experience of 13 cases of nonimmune hydrops fetalis.
So Ja JIN ; Kyung Yeun CHA ; Jong Duk KIM
Korean Journal of Perinatology 1991;2(2):68-74
No abstract available.
Hydrops Fetalis*
5.Etiology of hydrops fetalis at the Philippine General Hospital: A retrospective study
Michelle E. Abadingo ; Maria Melanie Liberty B. Alcausin
Acta Medica Philippina 2017;51(3):181-186
Objective:
Hydrops fetalis (HF) is a diagnosis with significant morbidity and mortality. It is the objective of this study to identify common etiologic causes of HF in the Philippine General Hospital (PGH).
Methods:
This is a retrospective review of hydrops fetalis cases delivered at the PGH from 2010 to 2014. There was a total of 75 identified cases of hydrops fetalis. However, only 58 of these, or 77.33% have available medical charts for review.
Results:
The median gestational age at birth was 31 (range 2140) weeks. There were 19 identified cases (32%) of stillbirth. Of the 32 patients born alive, 30 (93.75%) died in the immediate neonatal period. The etiologies of HF were identified in 15 cases, which included congenital anomalies (n=4), cardiac anomalies (n=3), infectious problems (n=3), hematologic anomalies (n=2), placental anomalies (n=2) and congenital tumor (n=1). Cases of congenital anomalies were only detected by congenital anomaly scan; no further work-ups were done. Fifteen (15) mothers presented with microcytic, hypochromic anemia on complete blood count (CBC). The cause of HF was not confirmed in the remaining 43 (74%) cases.
Conclusion
It is important to fully investigate the causes of HF to aid in the proper management and counseling. Further work-up must be done for mothers presenting with microcytic, hypochromic anemia. This is an important feature of alpha thalassemia. Partners of women suspected to have alpha thalassemia should also have a hematologic screening. The deletion of the four alpha genes will result to HB Bart’s hydrops fetalis; a major cause of hydrops fetalis in Southeast Asian countries.
Hydrops Fetalis
6.Nonimmune hydrops fetalis; an autopsy case.
Mi Sung CHUNG ; Young Mi KIM ; Mi Kyung KIM ; Shin Na KIM ; Keum Min PARK ; Song Ja JIN
Korean Journal of Perinatology 1992;3(2):109-116
No abstract available.
Autopsy*
;
Hydrops Fetalis*
7.Clinical Aspects of Hydrops Fetalis.
Korean Journal of Obstetrics and Gynecology 2000;43(8):1326-1330
No abstract available.
Edema*
;
Hydrops Fetalis*
8.A Case of Hydrops Fetalis due to Rh-Incompatibility.
Seong Kuk SEO ; Han Young JEONG ; Sung Won KIM ; Kil Hyun KIM
Journal of the Korean Pediatric Society 1989;32(2):256-261
No abstract available.
Edema*
;
Hydrops Fetalis*
9.A Case of Hydrops Fetalis due to Rh-Incompatibility.
Seong Kuk SEO ; Han Young JEONG ; Sung Won KIM ; Kil Hyun KIM
Journal of the Korean Pediatric Society 1989;32(2):256-261
No abstract available.
Edema*
;
Hydrops Fetalis*
10.A case of nonimmunologic hydrops fetalis.
Duck Rye KIM ; Hyun Young BAE ; Woo Yeol HWANG ; Hye Kyung YOO ; Yue Seung YANG ; Ho Soon JUNG
Korean Journal of Obstetrics and Gynecology 1993;36(11):3809-3813
No abstract available.
Edema*
;
Hydrops Fetalis*
Result Analysis
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