WordNet

of or relating to a fetus; "fetal development" (同)foetal

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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. 妊娠中のパルボウイルスB19感染parvovirus b19 infection during pregnancy [show details]
…fluid in the fetal soft tissues and serous cavities. The specific ultrasound findings of nonimmune hydrops fetalis are discussed elsewhere. The risk of anemia and fetal hydrops appears to be greater when…
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. 先天性代謝異常：疫学、病因、および臨床的特徴inborn errors of metabolism epidemiology pathogenesis and clinical features [show details]
…syndrome (mucopolysaccharidosis type I Hurler [MPS I H]) and GM1 gangliosidosis type 1 Nonimmune hydrops fetalis (abnormal fetal fluid collections) may occur in the following IEM : Lysosomal storage…

English Journal

Prevalence and risk factors for hearing loss in high-risk neonates in Germany.

Thangavelu K, Martakis K, Fabian S, Venkateswaran M, Roth B, Beutner D, Lang-Roth R.
Acta paediatrica (Oslo, Norway : 1992). 2019 Nov;108(11)1972-1977.
Hearing loss in infants is often diagnosed late, despite universal screening programmes. Risk factors of hearing impairment in high-risk neonates, identified from population-based studies, can inform policy around targeted screening. Our aim was to determine the prevalence and the risk factors of he
PMID 31074050

Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α-Thalassemia (- - deletion) Allele and Application for Double-Check Diagnosis of Hb Bart's Hydrops Fetalis Syndrome in Thailand.

Jomoui W, Tepakhan W, Karnpean R.
Hemoglobin. 2019 Oct;()1-5.
The α-thalassemia (α-thal) [- - (Southeast Asian) deletion] is highly prevalent in Southeast Asia and South China. The linkage between the single nucleotide polymorphism (SNP) rs77308790 and the - - deletion was reported in the Chinese population. This study reported the genotype of SNP rs77308790
PMID 31635494

[Genetic analysis of a family with recurrent hydrops fetalis and dilated cardiomyopathy].

Wu Q, Ma X, Shi H, Kong X, Ren S, Jiao Z.
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 2019 Oct;36(10)1028-1030.
To carry out genetic testing for a family with two pregnancies affected with hydrops fetalis and dilated cardiomyopathy (DCM) of the fetus. DNA was extracted from fetal tissue as well as peripheral blood samples from the couple. Single nucleotide polymorphism array (SNP array) and next-generation se
PMID 31598953

Japanese Journal

ヒトパルボウイルスB19感染により点状出血性発疹を伴う無形成発作を起こした遺伝性球状赤血球症の9歳男児例

青柳憲幸
日本小児血液・がん学会雑誌 56(2), 234-237, 2019
<p>ヒトパルボウイルスB19（PVB19）感染の臨床症状としては伝染性紅斑や，慢性溶血性貧血患者における無形成発作，非免疫性胎児水腫などが知られている．近年，PVB19感染に関連して，通常の発疹とは異なる点状出血性/紫斑性発疹がみられることがわかってきた．今回，躯幹中心に点状出血性発疹を認め，無形成発作を合併した遺伝性球状赤血球症（HS）の9歳男児というまれな症例を経験したので報告す …
NAID 130007705327

妊娠21週に診断した胎内サイトメガロウイルス感染の胎児超音波所見

早田桂,佐藤麻夕子,長治誠 [他],清水健治,小松玲奈,石田理,吉田信隆
現代産婦人科 = Modern trends in obstetrics & gynecology 60(2), 419-424, 2012-03-30
NAID 10030697742

羊水過多をきたし，胎児心不全に至った18cmの巨大胎盤血管腫の1例

自見倫敦,新小田真紀子,早川陽子 [他],大石哲也,辻本大治,中後聡,柴田貴志,徳田妃里,山本彩,登村正之,張友香,加藤大樹,奥杉ひとみ
産婦人科の進歩 64(4), 490-494, 2012
胎盤血管腫は胎盤に発生する良性腫瘍の中で最も頻度の高い疾患である．通常，腫瘍径は5cm以下のものが多く，15cmを超えるものはまれである<sup>1）</sup>．とくに腫瘍径の大きなものほど周産期合併症が多く，母体では羊水過多，早産，胎児では非免疫性胎児水腫，心不全，貧血，胎児発育不全，DICなどの重篤な合併症を引き起こすことが報告されている<sup>2,3） …
NAID 130003362641