Results 121 to 130 of about 116,640 (286)

De Novo Complex Genomic Rearrangement Spanning 2q31.1 in a Proband With Congenital Malformations: Genotype–Phenotype Correlation and Development of a CGR Detection Pipeline

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The 2q31 region is commonly associated with pathogenic alleles of the HOXD cluster leading to various clinical phenotypes related to skeletal development. We present a proband with tetralogy of Fallot and multiple congenital anomalies. Genomic variant screening including an in‐house CGR detection pipeline pairing genome sequencing (GS ...
Katherine Helle   +10 more
wiley   +1 more source

Association of maternal obesity and gestational weight gain with adverse maternal and perinatal outcomes

open access: yesJournal of the Pakistan Medical Association
Objective: To determine the association of maternal obesity and gestational weight gain with adverse maternal and perinatal outcomes. Method: The prospective, cross-sectional study was conducted from April 2023 to February 2024 at the Combined ...
Kurrat-Ul-Aaien   +5 more
doaj   +1 more source

GESTATIONAL WEIGHT GAIN DEPENDS ON THE INITIAL ANTHROPOMETRIC VALUES

open access: yesАкушерство, гинекология и репродукция, 2017
The aim was to study whether the increase in body weight during pregnancy depends on the initial anthropometric values. Materials and methods. This prospective study included 100 pregnant women; the measurements of their height, body weight, and BMI were
N. B. Chabanova   +2 more
doaj   +1 more source

Vitamin D and Birth Outcomes in Pregnancy [PDF]

open access: yes, 2016
Title: Vitamin D and Birth Outcomes in Pregnancy Purpose and Background/Significance: Vitamin D is essential for fetal growth and development and maternal wellbeing.
Sawka, Kristen
core  

Long‐Term Follow Up of Two Patients With Variants in the Cluster 1031‐1159 of TRRAP Gene: Expanding the Phenotype of Developmental Delay With or Without Dysmorphic Facies and Autism

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The transformation/transcription domain‐associated protein (TRRAP) gene encodes a large multidomain protein, a member of the phosphatidylinositol 3‐kinase‐related kinase (PIKK) family. TRRAP is a component of the histone acetyltransferase (HAT) complex, and it plays an important role in gene transcription, DNA repair, and cell‐cycle regulation.
Roseli Maria Zechi‐Ceide   +10 more
wiley   +1 more source

Reassessing the WIC Effect: Evidence from the Pregnancy Nutrition Surveillance System [PDF]

open access: yes
Recent analyses differ on how effective the Special Supplemental Nutrition Program for Women, Infants and Children (WIC) is at improving infant health.
Andrew D. Racine, Cristina Yunzal-Butler
core  

The Homozygous p.(Arg215Ter) Variant in XRCC2 Is Associated With Atypical Fanconi Anemia Without Major Hematological Abnormalities in Childhood

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli   +11 more
wiley   +1 more source

Maternal Weight after Childbirth versus Aging-Related Weight Changes [PDF]

open access: yes, 2017
Background Pregnancy weight gain is believed to contribute to female overweight and obesity. However, most studies do not account for the changes in body weight expected to occur as women age.
Kapinos, Kandice A   +2 more
core   +1 more source

Resolution of Refractory Multifocal Atrial Tachycardia in Costello Syndrome Using Trametinib: A Case Supporting MEK Inhibitors as Targeted, Specific Antiarrhythmic

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Arrhythmias affect approximately half of patients with Costello syndrome (CS, OMIM # 218040), with non‐reentrant atrial tachycardia being the most common. This case describes an infant with Costello syndrome carrying the pathogenic HRAS c.34G>A (p.G12S) variant who developed early‐onset, drug‐refractory multifocal atrial tachycardia (MAT ...
Vanina Taliercio   +11 more
wiley   +1 more source

Milestone Attainment in Young Children With Arthrogryposis Multiplex Congenita: Developmental Profile and Associated Factors

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Evidence on developmental milestones in children with arthrogryposis multiplex congenita (AMC) under the age of five is scarce. This multisite cross‐sectional study described developmental status and examined factors associated with milestone attainment in 143 children aged 0–66 months from a pediatric AMC Registry.
Ahlam Zidan   +13 more
wiley   +1 more source

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