نتایج جستجو برای: feeding difficulties

تعداد نتایج: 194982  

Journal: :Human molecular genetics 2010
Fabienne Schaller Françoise Watrin Rachel Sturny Annick Massacrier Pierre Szepetowski Françoise Muscatelli

The onset of feeding at birth is a vital step for the adaptation of the neonate to extra uterine life. Prader-Willi syndrome (PWS) is a complex neurogenetic disorder caused by the alteration of several imprinted contiguous genes including MAGEL2. PWS presents with various clinical manifestations, including poor suckling behaviour and feeding problems in neonates. Hypothalamic defects have been ...

2015
Linda Xavier Mangala Gowri

A Preexperimental study was done to assess the effectiveness of selected feeding techniques on knowledge and practice among caregivers. Purposive sampling technique was used and 35 caregivers were selected at “Anbu Illam” (Home for Cerebral Palsied children)-Vellore. Demographic variables were collected by using structured questionnaire and Observational checklist was used to assess the feeding...

Journal: :Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 2006
M K Caglar I Ozer F S Altugan

Data were prospectively obtained from exclusively breast-fed healthy term neonates at birth and from healthy mothers with no obstetric complication to determine risk factors for excess weight loss and hypernatremia in exclusively breast-fed infants. Thirty-four neonates with a weight loss > or = 10% were diagnosed between April 2001 and January 2005. Six of 18 infants who were eligible for the ...

Journal: :Journal of epidemiology and community health 1983
H J Wright P C Walker

A random sample of 617 primiparas was identified from birth notifications over a 12 month period and 534 of these were interviewed four weeks after confinement. Those breast feeding at the time of interview were contacted again at four months and those still breast feeding then were contacted at six and a half months. Duration of breast feeding was found to be significantly associated with five...

Journal: :Developmental medicine and child neurology 2010
Maria Clark Rebecca Harris Nicola Jolleff Katie Price Brian G R Neville

AIM Worster-Drought syndrome (WDS), or congenital suprabulbar paresis, is a permanent movement disorder of the bulbar muscles causing persistent difficulties with swallowing, feeding, speech, and saliva control owing to a non-progressive disturbance in early brain development. As such, it falls within the cerebral palsies. The aim of this study was to describe the physical and neuropsychologica...

Journal: :Journal of the Canadian Academy of Child and Adolescent Psychiatry = Journal de l'Academie canadienne de psychiatrie de l'enfant et de l'adolescent 2006
Hilary Le Page

A 17 year old young woman of borderline intellectual ability was referred to an outpatient mental health clinic from an inpatient adolescent unit following a 3 month admission. The diagnosis was of “First Episode Psychosis, possibly schizophrenia”. She was described as improving on olanzapine, and ready for discharge into the community. The Early Psychosis team made a visit to the adolescent in...

Journal: :Archives of disease in childhood. Fetal and neonatal edition 2003
L L LaGasse D Messinger B M Lester R Seifer E Z Tronick C R Bauer S Shankaran H S Bada L L Wright V L Smeriglio L P Finnegan P L Maza J Liu

OBJECTIVE To evaluate feeding difficulties and maternal behaviour during a feeding session with 1 month old infants prenatally exposed to cocaine and/or opiates. METHODS The study is part of the maternal lifestyle study, which recruited 11 811 subjects at four urban hospitals, then followed 1388 from 1 to 36 months of age. Exposure to cocaine and opiates was determined by maternal interview a...

Journal: :Children (Basel) 2023

Sotos syndrome is an autosomal dominant genetic disorder caused by mutations in the NSD1 gene. In this study, we report a case of preterm infant. The main clinical manifestations were severe bronchopulmonary dysplasia, congenital heart disease, difficulty feeding, and characteristic facial appearance. gene mutation was located at 177251854 on chromosome 5, identified as shear mutation, c.4765+1...

2016
Claire Kane Miller Lauren L. Madhoun

: http://p p://pubs.as The problems with feeding and swallowing that occur as a result of clefts and craniofacial anomalies range in severity. The extent of clefting, as well as other structural, airway, and neurologic issues, are factors that contribute to potential difficulty with oral feeding mechanics and with the integrity of airway protection during swallowing. Oral motor dysfunction in c...

2016
Jerilyn A. Smith

Background: Children with Autism Spectrum Disorder (ASD) frequently have feeding and eating difficulties as well as unusual responses to sensory stimuli. This can lead to significantly compromised occupational performance. Method: A secondary data analysis study design was used to investigate sensory processing characteristics as predictors of feeding and eating disturbances. Study subjects wer...

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