Results 91 to 100 of about 48,726 (248)

Novel OBSL1 Variant in a Chinese Patient with 3M Syndrome and the c.458dupG Mutation May Be a Potential Hotspot Mutation in the Chinese Population

open access: yesJCRPE
3M syndrome is an autosomal recessive disorder characterized by short stature and skeletal developmental abnormalities. A Chinese girl with 3M syndrome and a novel OBSL1 (obscurin-like 1 gene) variant is presented.
Yurong Piao   +4 more
doaj   +1 more source

Revesz syndrome

open access: yesRevista Brasileira de Oftalmologia, 2015
Revesz syndrome is a rare variant of dyskeratosis congenita and is characterized by bilateral exudative retinopathy, alterations in the anterior ocular segment, intrauterine growth retardation, fine sparse hair, reticulate skin pigmentation, bone marrow ...
Dayane Cristine Issaho   +4 more
doaj   +1 more source

Sociocultural and Structural Determinants of Black Maternal Mental Health: A Scoping Review

open access: yesBirth, EarlyView.
This image highlights the ways sociocultural and structural determinants intersect to influence Black maternal health and pathways to improving mental health of Black mothers and birthing parents. ABSTRACT Background Black women face a disproportionate risk of perinatal mental mood disorders with significant implications for maternal and infant health ...
Priscilla N. Boakye   +15 more
wiley   +1 more source

Intrauterine Growth Retardation and Nonalcoholic Fatty Liver Disease in Children

open access: yesInternational Journal of Endocrinology, 2011
Intrauterine growth retardation (IUGR), the most important cause of perinatal mortality and morbidity, is defined as a foetal growth less than normal for the population, often used as synonym of small for gestational age (SGA).
Anna Alisi   +3 more
doaj   +1 more source

THERAPY OF UROGENITAL INFECTIONS DURING PREGNANCY

open access: yesМедицинский совет, 2017
Urogenital infections (UGI) remain one of the urgent problems of obstetrics and gynecology. In the period of gestation, the UGI may cause such complications as chorioamnionitis, intrauterine growth retardation and intrauterine and intrapartum infection ...
V. L. Tyutyunnik   +3 more
doaj   +1 more source

Effects of prematurity and socio‐economic status on early life language exposure: A video coding study

open access: yesBritish Journal of Developmental Psychology, EarlyView.
Abstract Preterm birth is associated with later language impairment and delay. Socio‐economic deprivation is linked to decreased language exposure in early childhood, but it is unknown how prematurity influences this relationship. This study investigated the effects of socio‐economic status and gestational age at birth on language exposure, in a sample
Sinéad O'Carroll   +5 more
wiley   +1 more source

Seckel syndrome: A rare case report

open access: yesJournal of Indian Society of Pedodontics and Preventive Dentistry, 2014
Seckel syndrome (SS) is a rare, autosomal recessive syndrome; characterized by severe intrauterine and postnatal growth retardation, microcephaly, mental retardation, and typical facial appearance with beaklike protrusion of the midface (bird headed). In
Rinky Sisodia   +2 more
doaj   +1 more source

A Single Centre Study to Describe the Changes in Serum Testosterone Concentration Following Application of Testosterone Gel in Post‐Menopausal Women With Hypoactive Sexual Desire Disorder (HSSD) Already Receiving This as Part of Usual Care in Conjunction With Oestrogen‐Containing Hormone Replacement Treatment (HRT)

open access: yesClinical Endocrinology, EarlyView.
ABSTRACT Introduction Hypoactive Sexual Desire Disorder (HSDD) is characterized by a long‐term decrease in sexual desire (low‐libido) causing personal distress. HSDD predominantly affects post‐menopausal women or following oophorectomy. Despite the clear indication that testosterone action could overcome the symptoms of HSDD by elevating testosterone ...
Adrian Heald   +10 more
wiley   +1 more source

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