Articles with "failure thrive" as a keyword



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Optimizing cystectomy outcomes

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Published in 2019 at "Cancer"

DOI: 10.1002/cncr.32359

Abstract: In this month’s issue of Cancer, Smith et al from the University of North Carolina at Chapel Hill present a unique patient-centered perspective and identify potential solutions for reducing complications and subsequent readmissions after radical… read more here.

Keywords: failure thrive; readmission; optimizing cystectomy; cystectomy ... See more keywords
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A novel nonsense variant in the NFE2L1 transcription factor in a patient with developmental delay, hypotonia, genital anomalies, and failure to thrive

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Published in 2022 at "Human Mutation"

DOI: 10.1002/humu.24337

Abstract: The NFE2L1 transcription factor (also known as Nrf1 for nuclear factor erythroid 2‐related factor‐1) is a broadly expressed basic leucine zipper protein that performs a critical role in the cellular stress response pathway. Here, we… read more here.

Keywords: developmental delay; delay hypotonia; nfe2l1 transcription; factor ... See more keywords
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Diagnosis and treatment of gastric antral webs in pediatric patients

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Published in 2018 at "Surgical Endoscopy"

DOI: 10.1007/s00464-018-6338-2

Abstract: BackgroundGastric antral webs are mucosal structures, varying from fenestrated diaphragms to mucosal crescents, resulting in varying degrees of foregut obstruction. Patients commonly present with vomiting, failure to thrive, and abdominal pain. Prevalence is unknown, and… read more here.

Keywords: failure thrive; diagnosis; gastric antral; antral webs ... See more keywords
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Heterozygous mutations in the cholesterol side-chain cleavage enzyme gene (CYP11A1) can cause transient adrenal insufficiency and life-threatening failure to thrive

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Published in 2018 at "Hormones"

DOI: 10.1007/s42000-018-0048-y

Abstract: The first and rate-limited step of steroidogenesis in all steroidogenic tissues is the conversion of cholesterol to pregnenolone, catalysed by P450scc side-chain cleavage enzyme (CYP11A1 gene—SCC). SCC deficiency has been characterised as an autosomal recessive… read more here.

Keywords: cyp11a1; failure thrive; adrenal insufficiency; gene ... See more keywords
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Failure to Thrive, Hyponatremia, Hyperkalemia - Differential Diagnostic Reflections of a Rare Genetic Disease.

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Published in 2020 at "Klinische Padiatrie"

DOI: 10.1055/a-1031-9679

Abstract: Pseudohypoaldosteronism type I is a rare genetic disease of mineralocorticoid resistance that typically manifests in neonatal age. The patients are diagnosed with failure to thrive, dehydration, polyuria, vomiting, hyperkalemia, hyponatremia as well as potential metabolic… read more here.

Keywords: failure thrive; disease; genetic disease; type ... See more keywords
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A 6-Month-Old Infant with Severe Failure to Thrive during COVID-19 Pandemic

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Published in 2022 at "Clinical Chemistry"

DOI: 10.1093/clinchem/hvac012

Abstract: A 6-month-old male presented to the emergency department during the COVID-19 pandemic with 3-day history of fever, nasal congestion, cough, and decreased oral intake. He was not able to sit with support or roll over,… read more here.

Keywords: month old; severe failure; covid pandemic; failure thrive ... See more keywords
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Failure to Thrive in the PICU: An Overlooked Real Problem.

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Published in 2019 at "Pediatric Critical Care Medicine"

DOI: 10.1097/pcc.0000000000001986

Abstract: Unauthorized reproduction of this article is prohibited Copyright © 2019 by the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies. Unauthorized reproduction of this article is prohibited… read more here.

Keywords: critical care; medicine; picu; nutritional status ... See more keywords
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A novel homozygous variant in COX5A causes an attenuated phenotype with failure to thrive, lactic acidosis, hypoglycemia, and short stature

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Published in 2022 at "Clinical Genetics"

DOI: 10.1111/cge.14127

Abstract: Genetic defect in the nuclear encoded subunits of cytochrome c oxidase are very rare. To date, most deleterious variants affect the mitochondrially encoded subunits of complex IV and the nuclear genes encoded for assembly factors.… read more here.

Keywords: lactic acidosis; thrive lactic; cox5a; failure thrive ... See more keywords
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A syndrome of severe intellectual disability, hypotonia, failure to thrive, dysmorphism, and thinning of corpus callosum maps to chromosome 7q21.13‐q21.3

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Published in 2022 at "Clinical Genetics"

DOI: 10.1111/cge.14143

Abstract: Six individuals of consanguineous Bedouin kindred presented at infancy with an autosomal recessive syndrome of severe global developmental delay, positive pyramidal signs, unique dysmorphism, skeletal abnormalities, and severe failure to thrive with normal birth weights.… read more here.

Keywords: intellectual disability; corpus callosum; syndrome severe; thinning corpus ... See more keywords
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Failure to thrive among asylum-seeking children: A descriptive study from Turkey.

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Published in 2023 at "Public health nursing"

DOI: 10.1111/phn.13199

Abstract: OBJECTIVE The aim of the study was to determine failure to thrive among asylum-seeking children. DESIGN The study was a descriptive study. SAMPLE The sample of the study comprised of 187 children who were registered… read more here.

Keywords: thrive among; asylum seeking; seeking children; among asylum ... See more keywords
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Myxedema Coma due to Hashimoto Thyroiditis: A Rare but Real Presentation of Failure to Thrive in Infancy

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Published in 2018 at "Hormone Research in Paediatrics"

DOI: 10.1159/000488467

Abstract: Background: Hashimoto thyroiditis (HT) is uncommon in infancy, and myxedema coma (MC) is even less common. While prior reports have documented these entities separately, to our knowledge, MC in combination with HT has not been… read more here.

Keywords: myxedema coma; failure thrive; infancy; hashimoto thyroiditis ... See more keywords