Results 51 to 60 of about 44,865 (296)

First cases of exclusive paternal care in stink bugs (Hemiptera: Pentatomidae)

Zoologia (Curitiba), 2010
We describe paternal care in two pentatomid bugs, Lopadusa (Lopadusa) augur Stål, 1860 and Edessa nigropunctata Berg, 1884. Field and laboratory observations showed that males remain with their eggs and early hatched nymphs, while females abandon the ...
Gustavo S. Requena, Taís M. Nazareth, Cristiano F. Schwertner, Glauco Machado   +3 more
doaj   +1 more source

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons   +6 more
wiley   +1 more source

Sociodemographic profile and participation in the daily care of children with microcephaly

Cadernos Brasileiros de Terapia Ocupacional, 2019
Introduction: The family lives sociocultural transformations requesting more of the man in the children’s daily cares with deficiency because commonly the mothers wrap up in the tasks causing an overload in the daily tasks.
Tainá Alves Rocha da Cruz, Emanuele Mariano de Souza Santos, Flávia Calheiros da Silva, Monique Carla da Silva Reis, Ângela Cristina Dornelas da Silva   +4 more
doaj   +1 more source

Paternal factors and adverse birth outcomes in Lanzhou, China

BMC Pregnancy and Childbirth, 2021
Background Many maternal factors are known to be associated with adverse birth outcomes, but studies about paternal factors yielded inconsistent conclusions.
Jing Li, Jie Qiu, Ling Lv, Baohong Mao, Lei Huang, Tao Yang, Cheng Wang, Qing Liu   +7 more
doaj   +1 more source

Expectant fathers’ health behaviors, infant care intentions, and social-emotional wellbeing in the perinatal period: A latent class analysis and comparison to mothers

Preventive Medicine Reports, 2023
While parental behaviors during the ‘first thousand days’ are critical for child health, little is known about fathers during this time. We examined prenatal patterns of health behaviors, social-emotional wellbeing, and infant care intentions among ...
Rachel C. Whooten, Milton Kotelchuck, Ariadne V. Caballero Gonzalez, Nafissa Johnson, Gracia Kwete, Man Luo, Haley Farrar Muir, Elizabeth A. Barth, Nicole Smith, Elsie M. Taveras   +9 more
doaj   +1 more source

Noonan Syndrome Spectrum Disorders Predispose to Systemic Lupus Erythematosus: Case Report and Critical Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT RASopathies are clinically overlapping neurodevelopmental syndromes resulting from germline mutations in genes involved in the rat sarcoma/mitogen‐activated protein kinases (RAS/MAPK) pathway. Historically, RASopathies have been described by clinical phenotypes, such as Noonan syndrome and Neurofibromatosis type I.
Anastasia‐Vasiliki Madenidou, Gillian I. Rice, James O'Sullivan, Ben Parker, Ian N. Bruce, Emma Burkitt‐Wright, Tracy A. Briggs   +6 more
wiley   +1 more source

KDM2B‐Related Neurodevelopmental Disorder A Case‐Series Supporting the CxxC Domain Phenotype With Emphasis on Ocular and Dermatologic Features

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The KDM2B‐related neurodevelopmental disorder is a recently identified Mendelian disorder of the epigenetic machinery associated with pathogenic variants in KDM2B. Global developmental delay, intellectual disability, congenital anomalies, and systemic manifestations characterize the disorder.
Adriana Gomes, Álvaro Martín‐Rodríguez, Miguel Del Campo, Lynne M. Bird   +3 more
wiley   +1 more source

Examination of Turkish University Students’ Internet Addiction in Relation to Their Parental Attachment Styles and Sociodemographics

SAGE Open, 2019
The purpose of this study was to examine university students’ Internet addiction in relation to their parental attachment and sociodemographics. The participants consisted of 402 university students aged 17 to 25 years, 249 (61.9%) of whom were female ...
Hatice Kumcağız
doaj   +1 more source

The First Reported Case of an Inherited Pathogenic Variant in DEAF1 From a Parent With Milder Phenotype Provides Evidence of Variable Gene Expressivity of the DEAF1‐Associated Vulto‐van Silfout‐de Vries Syndrome (VSVS)

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT DEAF1‐associated neurodevelopmental disorder (DAND) is a neurodevelopmental spectrum disorder caused by two methods of inheritance: the autosomal dominant intellectual disability syndrome (Vulto‐van Silfout‐de Vries syndrome (VSVS), OMIM #615828), and the autosomal recessive Neurodevelopmental disorder with hypotonia and impaired expressive ...
Kylie Katz, Philip Jensik, Milen Velinov
wiley   +1 more source

Certainty of paternity in two coucal species with divergent sex roles: the devil takes the hindmost

BMC Evolutionary Biology, 2018
Background Certainty of paternity is considered an important factor in the evolution of paternal care. Several meta-analyses across birds support this idea, particularly for species with altricial young. However, the role of certainty of paternity in the
Ignas Safari, Wolfgang Goymann
doaj   +1 more source