Results 121 to 130 of about 2,332 (179)

De novo reciprocal translocation t(5;11)(q22;p15) associated with hydrops fetalis (reciprocal translocation and hydrops fetalis)

, 2015
Objective: This is a case of a prenatally diagnosed non-immune hydrops fetalis (NIHF) associated with translocation t(5;11)(q22;p15). An association between NIHF and this translocation has not been reported previously.; Case Report: The patient was ...
Artunc-Ulkumen B., Baytur Y.B., Bal F., Pala H.G., Uyar Y., Koyuncu F.M.   +5 more
core   +1 more source

Hydrops fetalis associated with erythrocyte pyruvate kinase deficiency

, 2000
The authors report a case of hydrops fetalis due to severe pyruvate kinase deficiency, the most unusual clinical manifestation of this disease. Conclusion Pyruvate kinase deficiency, as other erythrocyte enzymopathies, must be considered in the ...
Costa, Elísio, Costa, Ricardo, Dias, Clara Paz, Ferreira, Paula, Araújo, Filomena, Vilarinho, António, Resende, C., Morais, Lurdes, Barbot, José   +8 more
core  

Non immune hydrops fetalis due to Parvovirus B19 infection. A case report

, 2023
Backround: The term "hydrops fetalis" refers to excessive accumulation of pathologic serous fluid within the fetal soft tissues and body cavities. There are two categories, the immune and the nonimmune hydrops (NIHF).
Fasoulakis, Zacharias, Daskalakis, George, Antsaklis, Panos, Chatziioannou, Maria Ioanna, Theodora, Marianna   +4 more
core  

Hydrops Fetalis.

Hydrops fetalis is a severe, life-threatening fetal condition, characterized by abnormal fluid accumulation in two or more fetal compartments. This thesis focuses on both immune and non-immune hydrops fetalis (NIHF), with the emphasis on the latter due ...
Rehmann, Felicitas,
core  

Prenatally diagnosed lethal type Larsen-like syndrome associated with bifid tongue

The Turkish Journal of Pediatrics, 2008
Larsen syndrome is characterized by multiple joint dislocations, associated with a typical facial appearance and frequently other abnormalities. Both dominant and recessive patterns of inheritance have been reported.
Diclehan Orhan, Sevim Balci, Ozgür Deren, Eda Gülen Utine, Ahmet Başaran, Gülsev Kale   +5 more
doaj  

[Whole exome sequencing analysis of compound heterozygous variants of CDAN1 gene in a Chinese family with non-immune hydrops fetalis]. [PDF]

Nan Fang Yi Ke Da Xue Xue Bao, 2021
Wang Y, Li Q, Sun X, Li S, He J, Zhang M, Huang L, He W.   +7 more
europepmc   +1 more source

Non-immunological hydrops fetalis

, 2017
A case of hydrops fetalis which was not due to isoimmunization is presented. The condition was diagnosed antenatally by means of Ultrasonography and the infant was delivered at 32 weeks' gestation.
Riseborough, Jennifer, Riley, P., Wittenberg, D.F.   +2 more
core  

A preterm neonate with fetal anemia and immune hydrops fetalis requiring intrauterine transfusion and postnatal exchange transfusion: a case report

Hydrops fetalis is a presenting illness with various immune and non-immune etiologies. It involves fluid accumulation in body cavities, and symptoms specific to its underlying cause.
Mehta, Ashish, Shah, Binoy, Mehta, Abhijit, Shah, Manish, Patel, Bhavya   +4 more
core   +1 more source

Immune and non-immune hydrops fetalis in a resource-limited setting: a report of two cases. [PDF]

Pan Afr Med J
Ochieng WO, Chemwey RN, Lagat MK, Thagana EK.   +3 more
europepmc   +1 more source

Case Report of Meconium Peritonitis: A Rare Cause of Non-immune Hydrops Fetalis. [PDF]

Cureus
Maddali R, Alvarez-Gell C, Balasundaram P, Sakr M.   +3 more
europepmc   +1 more source