Results 61 to 70 of about 8,139 (215)

Molecular cytogenetic analysis of a hydatidiform mole with coexistent fetus: a case report

open access: yesJournal of Medical Case Reports, 2019
Background A hydatidiform mole with a coexisting fetus is a rare condition that commonly occurs as either a partial mole with fetus or a twin pregnancy comprising a complete mole and normal fetus.
Nozomi Uemura   +8 more
doaj   +1 more source

Hydatidiform mole and gestational trophoblastic disease [PDF]

open access: yes, 2009
A mola hidatiforme é uma complicação relativamente infrequente da gravidez, mas com potencial para evolução para formas que necessitam de tratamento sistêmico e podem ser ameaçadoras da vida.
ANDRADE, Jurandyr Moreira de
core   +2 more sources

Patient Satisfaction With Centralising Care of Gestational Trophoblastic Disease in Western Australia: A Descriptive Cross‐Sectional Evaluation

open access: yesEuropean Journal of Cancer Care, Volume 2026, Issue 1, 2026.
Introduction Gestational trophoblastic neoplasia (GTN) is a rare, malignant form of gestational trophoblastic disease (GTD), and international guidelines recommend centralisation of care for best outcomes. The Western Australian Trophoblastic Centre (WATC) was established in 2023 aiming to provide centralised, person‐centred care coordinated by a ...
Natalie Williams   +5 more
wiley   +1 more source

An Incidental Ultrasonographic Diagnosis of Partial Hydatidiform Mole in a Old Primigravida: A Case Report

open access: yesJournal of Nepal Medical Association, 2020
Hydatidiform mole is an abnormal pregnancy common in Asian populations compared to western countries; however, a partial hydatidiform mole is relatively uncommon and very challenging to diagnose on ultrasound.
Sudeep Thapa, Ramesh Rana, Sheela Kumari
doaj   +1 more source

Downregulation of the Gli Transcription Factors Regulator Kif7 Facilitates Cell Survival and Migration of Choriocarcinoma Cells [PDF]

open access: yes, 2014
published_or_final_versio
Chan, KKL   +5 more
core   +1 more source

Downregulation of Chromosome 19 miRNA Cluster and the Tumor‐Suppressive Role of miR‐517a‐3p in Choriocarcinoma

open access: yesCancer Science, Volume 116, Issue 12, Page 3473-3486, December 2025.
Chromosome 19 microRNA cluster was downregulated in choriocarcinoma compared with complete hydatidiform mole. miR‐517a‐3p reduced the proliferation, migration, and invasion abilities of choriocarcinoma cell lines. Downregulation of SRSF1, targeted by miR‐517a‐3p, suppressed the malignant potential of choriocarcinoma cell lines. ABSTRACT Choriocarcinoma
Yuki Nishiko   +14 more
wiley   +1 more source

Normally Developing Pregnancy and Hydatidiform Mole: A Case Report

open access: yesИнновационная медицина Кубани
Introduction: Hydatidiform mole with a normally developing fetus is a rare case associated with an increased risk of bleeding, preterm birth, preeclampsia, congenital anomalies, and intrauterine fetal death.Case report: We report a case of a twin ...
A. V. Peredvigina   +6 more
doaj   +1 more source

Molar Pregnancy Presents as Tubal Ectopic Pregnancy [PDF]

open access: yesInternational Journal of Fertility and Sterility, 2011
Hydatidiform moles are abnormal gestations characterized by the presence of hydropic changes affecting some or all of the placental villi. Hydatidiform moles arise as a result of the fertilization of an abnormal ovum. In this report, the patient was a 29
Fatemeh Davari Tanha   +3 more
doaj  

Hydatidiform molar pregnancy presenting with preeclampsia in 6th weeks of pregnancy: a case report [PDF]

open access: yesMajallah-i Zanān, Māmā̓ī va Nāzā̓ī-i Īrān, 2018
Introduction: preeclampsia is one of the rare symptoms of molar pregnancy and is more prevalent in pregnancies with large volumes of abnormal trophoblastic tissue. Preeclampsia is associated with hypertension and proteinuria and rarely occurs in patients
Laya Shirinzadeh   +6 more
doaj   +1 more source

Six New Cases of 22q13.2 Gain Including TFC20: First Report of Triplication and Smallest Duplication Associated With Neurodevelopmental Delays

open access: yesClinical Genetics, Volume 108, Issue 6, Page 731-741, December 2025.
This study reports six new cases of 22q13.2 duplication and triplication, including the TCF20 gene, associated with neurodevelopmental disorders and various morphological and systemic abnormalities. The findings suggest a variable expressivity, but their complete penetrance remains uncertain compared to well‐established loss‐of‐function variants ...
Etienne Bizot   +13 more
wiley   +1 more source

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