Results 21 to 30 of about 15,713 (161)

Focus on Prenatal Detection of Micrognathia [PDF]

open access: yes, 2019
Fetal micrognathia involves abnormal or arrested development of the fetal mandible. Till recently, the prenatal diagnosis was subjective, based on the evaluation of the fetal profile and assessment of the relationship between the maxilla and the mandible.
Antonakopoulos, N, Bhide, A
core   +1 more source

Severe polyhydramnios: incidence of anomalies [PDF]

open access: yesAmerican Journal of Roentgenology, 1987
The sonograms of 195 singleton pregnancies complicated by polyhydramnios were reviewed, and follow-up information was obtained on 191 patients. A grading system was developed that differentiated mild from severe polyhydramnios using real-time or static sonographic equipment.
S Z, Barkin   +5 more
openaire   +2 more sources

MFM Guidance for COVID-19 [PDF]

open access: yes, 2020
The World Health Organization (WHO) has declared COVID-19 a global pandemic. Healthcare providers should prepare internal guidelines covering all aspect of the organization in order to have their unit ready as soon as possible.
Bellussi, Federica   +3 more
core   +1 more source

Isolated foetal ascites. [PDF]

open access: yes, 2001
The prenatal diagnosis and perinatal outcome of two patients with isolated foetal ascites compatible with chyloperitoneum is described. The foetal ascites resolved spontaneously after delivery with good perinatal outcome in both cases.
Lam, YH, Leung, WC, Tang, MH
core  

Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy [PDF]

open access: yes, 2014
Peer ...
Adele D’Amico   +73 more
core   +1 more source

Gestational diabetes [PDF]

open access: yes, 2017
Gestational diabetes mellitus (GDM) is defined as hyperglycaemia that is diagnosed for the first time in the second or third trimester of pregnancy. It occurs in 1 in 7 pregnancies worldwide and is associated with increased risk of adverse perinatal ...
Murphy, Helen R.   +2 more
core   +1 more source

A Case of Monochorionic-Diamniotic Twin Pregnancy with Polyhydramnios-Polyhydramnios Sequence

open access: yesJournal of Nippon Medical School, 2009
We present a case of monochorionic-diamniotic (MD) twin pregnancy with polyhydramnios-polyhydramnios sequence. A 20-year-old woman, gravida 1, para 0, was referred to our hospital at 31 weeks and 6 days' gestation for consultation about a high-risk pregnancy due to the presence of discordant fetal growth pattern (26% of fetal growth discordance) with ...
Yusuke, Inde   +5 more
openaire   +3 more sources

Acute Polyhydramnios Complicating Twin Pregnancies [PDF]

open access: yes, 2017
Acute polyhydramnios in the second trimestr is a typical complication in monozygous twin pregnancies. It is caused by a feto-fetal transfusion with anemia on the donor and polycytemia on the recipient twin. Contrary to the chronic hydramnios, there is no
Huch, A.   +3 more
core  

Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis. [PDF]

open access: yes, 2019
BACKGROUND: Bartter Syndrome is a rare, genetically heterogeneous, mainly autosomal recessively inherited condition characterized by hypochloremic hypokalemic metabolic alkalosis.
A Bettinelli   +49 more
core   +3 more sources

Novel mutation in CCBE 1 as a cause of recurrent hydrops fetalis from Hennekam lymphangiectasia-lymphedema syndrome-1. [PDF]

open access: yes, 2018
Whole exome sequencing (WES) was used to determine the etiology of recurrent hydrops fetalis in this case of Hennekam lymphangiectasia-lymphedema syndrome-1.
Andreasen, Tara S   +7 more
core  

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