نتایج جستجو برای: diamniotic

تعداد نتایج: 404  

Journal: :Arquivos de neuro-psiquiatria 2016
Denise Campos Amabile V Arias Thatiane M Campos-Zanelli Daniela S Souza Orlando G Dos Santos Neto Cleisson Fabio A Peralta Marilisa M Guerreiro

OBJECTIVE To assess the neurodevelopmental functions of survivors of twin-twin transfusion syndrome (TTTS) treated by fetoscopic laser coagulation (FLC), during the first year of life, comparing them to a control group; and to verify the influence of specific variables on neurodevelopment. METHOD This was a prospective, longitudinal study. The sample comprised 33 monochorionic diamniotic twin...

2015
Hidehiko Maruyama Takeshi Inagaki Yusei Nakata Akane Kanazawa Yuka Iwasaki Kiyoshi Sasaki Ryuhei Nagai Hiromi Kinoshita Jun Iwata Kiyoshi Kikkawa

Introduction This report will discuss a case of minimally conjoined omphalopagus twins (MCOTs) with a body stalk anomaly (BSA). Case Report We experienced monochorionic diamniotic (MD) twins born at 31 weeks. One infant was suspicious of BSA before birth, and another infant was normal. But normal infant had anal atresia with small intestine which was inserted behind the umbilicus. Twins had ver...

Journal: :Nihon Ika Daigaku zasshi 1999
S Suzuki S Okudaira R Sawa Y Yoneyama H Asakura S Shin K Kaneko T Araki

The goal of this study was to assess the characteristics of monochorionic-diamniotic (MD) growth-retarded twin infants with twin-twin transfusion syndrome (TTTS) compared with those without TTTS during the third trimester. Retrospective analyses of the growth patterns and amniotic fluid volumes were performed on 5 MD twin pregnancies in which one or both twins showed growth retardation with TTT...

Journal: :Acta medica portuguesa 2017
Emídio Vale-Fernandes Joana Dias Belandina Gil Alexandra Cadilhe

The incidence of single fetal death in twin pregnancy varies from 0.5% - 6.8%, leaving the surviving fetus with increased morbi-mortality. The prognosis is worse in monochorionic pregnancies. In addressing these cases it should be noted referral to tertiary center with differentiated perinatal support, induction of fetal lung maturation and termination of pregnancy if there's loss of fetal well...

2013
Arzu Doruk Ilay Gozukara Güneş Burkaş Esin Bilik Talat Umut Kutlu Dilek

Abnormal fusion of the Müllerian ducts or failure of resorption of the septum causes varying degrees of congenital uterine malformation. They are often associated with reproductive problems such as miscarriage, premature labour, premature rupture of the membranes, or malpresentation. Twin gestation in a case of bicornuate uterus is extremely rare. A 37-year-old multiparous woman conceived a twi...

Journal: :Puerto Rico health sciences journal 2016
Ronald López-Cepero Joseph Santoro Alberto de la Vega

Feto-fetal transfusion syndrome is a pathological process unique to diamniotic monochorionic pregnancies. It is the consequence of an unbalanced fetal blood flow through communicating vessels within a shared placenta. When it occurs, a polyuric, hypervolemic recipient twin co-exists with a hypovolemic oliguric donor. The presence of polyhydramnios or oligohydramnios is considered a poor prognos...

Journal: :Irish medical journal 2015
M Boyle A Lyons S Ryan F Malone A Poran

Untreated twin-twin transfusion syndrome (TTTS) is associated with significant mortality and neurological impairment. Fetoscopic laser surgery (FLS) is the treatment of choice. We sought to assess intracranial abnormalities in TTTS twins following treatment. In this prospective, blinded study MRI scans were performed on 3 groups; (1) monochorionic diamniotic (MCDA) twins with TTTS who had under...

2013
David N. Hackney Nahla Khalek Julie Moldenhauer Tulin Ozcan

The presence of polyhydramnios and oligohydramnios is pathognomonic for twin-twin transfusion syndrome (TTTS). However, polyhydramnios of both twins can exist in TTTS in the setting of a septostomy of the dividing membrane. In prior reported cases of dual polyhydramnios TTTS, the septostomy was identified through either ultrasound or fetoscopy thus helping to establish the diagnosis of TTTS wit...

Journal: :Indian pediatrics 1981
B Bhandari S L Mandowara R Mehta

Meckel-Gruber syndrome is a rare lethal autosomal recessive condition which was first described by Johann Friedrich Meckel in 1822 and GB Gruber in 1934. More than 200 cases have been reported worldwide with an incidence ranging from 1:13,250 to 1:140,000 live births. A 21-year-old female with G3 A2 L0, presented with twin pregnancy with history of previous two anencephalic pregnancies. The pre...

2016
Jin Young Bae Jin Ju Oh Seong Yeon Hong

Twin anemia-polycythemia sequence (TAPS) is characterized by a wide discrepancy of hemoglobin between two monochorionic fetuses without sign of twin oligo-polyhydramnios sequence. A primiparous woman with monochorionic diamniotic twin transferred for preterm labor. Ultrasonographic evaluation at 32+3 weeks of gestation revealed increased middle cerebral artery-peak systolic velocity (77.4 cm/se...

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