Results 71 to 80 of about 16,543 (245)

Polyhydramnios as a Predictor of Adverse Pregnancy Outcomes

Sultan Qaboos University Medical Journal, 2013
Objectives: This study aimed to ascertain the frequency of polyhydramnios in singleton pregnancies, to determine the associated risk factors, and assess the adverse maternal and perinatal outcomes.
Kaukab Tashfeen, Ilham Moosa Hamdi
doaj  

Antenatal Bartter Syndrome as a Rare Cause of Severe Polyhydramnios: A Case Report and Review of the Literature

Clinical Case Reports
Severe polyhydramnios occurs in 1%–2% of pregnancies and may be associated with maternal diabetes, fetal structural anomalies, genetic disorders, or remain idiopathic. Among the rare etiologies is Bartter syndrome, a renal tubular defect causing impaired
Fatemeh Shariati nia, Atefe Hashemi, Shaghayegh Moradi Alamdarloo, Maryam Kasraeian, Dorna Derakhshan, Hamide Barzegar   +5 more
doaj   +1 more source

Polyhydramnios is associated with postnatal dysphagia determining short-term prognosis of the newborn with 22q11.2 deletion syndrome - A case series analysis

Taiwanese Journal of Obstetrics & Gynecology, 2020
Objective: We experienced a case of 22q11.2 deletion syndrome (22qDS), with severe polyhydramnios, and dysphagia, which prompted us to review prognosis in neonates with 22qDS, with a focus on dysphagia. Case report: A patient was referred to our hospital
Tamae Nabeshima, Tatsuya Fujii, Takeshi Nagamatsu, Ayako Hashimoto, Takahiro Seyama, Kaori Kubota, Seisuke Sayama, Toshio Nakayama, Keiichi Kumasawa, Takayuki Iriyama, Yutaka Osuga, Tomoyuki Fujii   +11 more
doaj   +1 more source

Metabolic Profile and Neurogenic Potential of Human Amniotic Fluid Stem Cells From Normal vs. Fetus-Affected Gestations

Frontiers in Cell and Developmental Biology, 2021
Human amniotic fluid stem cells (hAFSCs) possess some characteristics with mesenchymal stem cells (MSCs) and embryonic stem cells and have a broader differentiation potential compared to MSCs derived from other sources.
Giedrė Valiulienė, Aistė Zentelytė, Elizabet Beržanskytė, Rūta Navakauskienė   +3 more
doaj   +1 more source

Successful propranolol therapy for infantile hepatic hemangioma with cardiac failure

JPGN Reports, EarlyView.
Abstract Infantile hepatic hemangioma (IHH) can cause severe complications such as high‐output cardiac failure and growth faltering, requiring prompt diagnosis and intervention. In the absence of standardized treatment guidelines, propranolol has emerged as an effective and well‐tolerated therapy.
Fadhel Al Ateeqi, Ala K. Shaikhkhalil, Haitham Talo, Naeem Jagirdar, Mahdia AL‐Haidar   +4 more
wiley   +1 more source

Maximum Vertical Pocket Versus Amniotic Fluid Index: Assessing Adverse Pregnancy Outcomes in Patients With Polyhydramnios

Reproductive, Female and Child Health
Objectives To describe differences in outcomes in pregnancies complicated by polyhydramnios based on whether the diagnosis was made by maximum vertical pocket (MVP), amniotic fluid index (AFI) or both.
Alexandria C. Kraus, Lauren M. Kucirka, Hina Shah, Juan C. Prieto, Jeffrey S. A. Stringer, Nancy C. Chescheir, Tracy A. Manuck, Kim A. Boggess   +7 more
doaj   +1 more source

Investigation of the Effect of Amniotic Fluid Index on Pregnancy Consequences in Pregnant Women Referring to Shahidan Mobini Hospital, Sabzevar, 2015

مجله علمی دانشگاه علوم پزشکی کردستان, 2023
Background and Aim: Amniotic fluid is an effective indicator for placental function and fetal development. Evaluating amniotic fluid volume is one of the main ways to assess fetal health.
roya baghani, nasim pajohan
doaj  

Airway Involvement in Conradi–Hünermann–Happle Syndrome: A Novel Clinical Manifestation

The Laryngoscope, EarlyView.
We report the first documented case of airway involvement in Conradi–Hünermann–Happle syndrome (CDPX2), an X‐linked dominant form of chondrodysplasia punctata caused by pathogenic variants in EBP. A 2‐month‐old female with genetically confirmed CDPX2 developed severe subglottic stenosis and persistent respiratory distress requiring CPAP; cross ...
Enrique G. Villarreal, Jackie Chiang, Evan J. Propst, Nikolaus E. Wolter   +3 more
wiley   +1 more source

A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment. [PDF]

, 2017
Megalencephaly and macrocephaly present with a head circumference measurement 2 standard deviations above the age-related mean. However, even if pathologic events resulting in both megalencephaly and macrocephaly may coexist, a distinction between these ...
Corsello G, Falsaperla R, Parano E, Pavone P, Praticò AD, Rizzo R, Ruggieri M   +6 more
core   +1 more source

Yield of Whole Genome Sequencing for Pathogenic Single Nucleotide Variants in Congenital Heart Disease: A Systematic Review and Meta‐Analysis

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective This systematic review and meta‐analysis aimed to assess the diagnostic yield of pathogenic or likely pathogenic (P/LP) single nucleotide variants (SNVs) using whole genome sequencing (WGS) in congenital heart disease (CHD). Methods A systematic search of three databases (2000–2024) was conducted, and two reviewers independently ...
Hiba J. Mustafa, Parisa Najjariasl, Faezeh Aghajani, Enaja V. Sambatur, Andrew Rodenbarger, Stephanie Guseh, Amy E. Roberts, Alireza A. Shamshirsaz   +7 more
wiley   +1 more source