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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2019/12/27 06:52:22」(JST)

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1. 非免疫性胎児水腫nonimmune hydrops fetalis [show details]
…cavities. Nonimmune hydrops fetalis (NIHF) comprises the subgroup of cases not caused by red cell alloimmunization (eg, RhD, Kell). Multiple fetal anatomic and functional disorders can cause NIHF. This topic …
2. 胎児水腫の生後ケアpostnatal care of hydrops fetalis [show details]
…mother and fetus. Nonimmune − Nonimmune hydrops fetalis (NHF) is associated with numerous disorders that include cardiac, pulmonary, infectious, and genetic etiologies NHF accounts for almost 90 percent …
3. 羊水過多polyhydramnios [show details]
4. 新生児に生じる胸水の病因、臨床症状、診断、評価etiology clinical manifestations diagnosis and evaluation of pleural effusions in the neonate [show details]
…metabolic disorders, anemia, and infection A more detailed discussion on the etiology of nonimmune hydrops fetalis is found separately. Neonatal chylothorax results from the accumulation of chyle in the…
5. 胎児母体間大量自然出血spontaneous massive fetomaternal hemorrhage [show details]
…and FMH exceeded 20 mL/kg (30 percent of blood volume) in 79 percent of cases . Nonimmune hydrops fetalis (NIHF) – NIHF may be discovered incidentally during prenatal sonography performed for standard …

Hydrops fetalis in a cohort of 3,137 stillbirths and second trimester miscarriages.

, M M, E E, E E, h h, .
American journal of medical genetics. Part A. 2019 Dec;179(12)2338-2342.
Hydrops fetalis was diagnosed in 277 (9%) of 3,137 fetuses referred to the Wisconsin Stillbirth Service Program (WiSSP) for etiologic evaluation of stillbirth or second trimester miscarriage. Hydrops was clinically recognized at delivery in only about half the cases, while the remainder were diagnos
PMID 31512356

Pathway to diagnosis and burden of illness in mucopolysaccharidosis type VII - a European caregiver survey.

Morrison A, Oussoren E, Friedel T, Cruz J, Yilmaz N.
Orphanet journal of rare diseases. 2019 Nov;14(1)254.
Mucopolysaccharidosis type VII (Sly disease, MPS VII), is an ultra-rare, multi-symptom disease with variable clinical presentations which can present challenges with diagnosis, management and care. We believe this survey is the first to explore the patient experience through direct questioning of th
PMID 31727109

Prenatally Diagnosed Congenital Ventricular Outpouchings: An Institutional Experience and Review of the Literature.

Shuplock JM, Kavanaugh-McHugh A, Parra D.
Pediatric cardiology. 2019 Nov;().
Congenital ventricular outpouchings (CVOs) are rare congenital heart defects with limited data regarding prognosis and outcomes. We aimed to describe the characteristics, outcomes and factors associated with morbidity and mortality of prenatally diagnosed CVOs using our institutional experience and
PMID 31728571