Article

Genetic manifestations and phenotype spectrum of feeding difficulty of unknown etiology: a hospital-based cohort study

2022-10-06

Abstract excerpt

<title>Abstract</title> <p>Background Feeding difficulties of unknown etiology are often combined with multiple system disorders caused by rare genetic diseases that are difficult to diagnose only based on clinical manifestations. In this study, we aimed to investigate the genetic causes of feeding difficulty of unknown etiology. Methods Patients during 2018-10 to 2022-5 diagnosed with feeding difficulty at our...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 5632eafe-57d6-5c55-a4d2-aae2bcdfe116
DOI: 10.21203/rs.3.rs-2113524/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Genetic manifestations and phenotype spectrum of feeding difficulty of unknown etiology: a hospital-based cohort studyDOI 10.21203/rs.3.rs-2113524/v1Read

Genetic Manifestations and Phenotype Spectrum in Infants With Feeding Difficulty.Semantic proximity Read

The Genetic Architecture of Congenital Diarrhea and EnteropathySemantic proximity Read

Gaps in the phenotype descriptions of ultra-rare genetic conditions: review and multicenter consensus reporting guidelinesSemantic proximity Read

Diagnostic yield and clinical utility of whole-exome sequencing in pediatric patients with rare and undiagnosed diseases: a prospective, single-center study from the Czech RepublicSemantic proximity Read

Gastrointestinal and feeding difficulties in CHARGE syndrome: A review from head-to-toe.Semantic proximity Read

Mapping the diagnostic odyssey of congenital disorders of glycosylation (CDG): insights from the communitySemantic proximity Read

Clinical utility in infants with suspected monogenic conditions through next‐generation sequencingSemantic proximity Read

Genetic background and clinical characteristics of infantile hyperammonaemiaSemantic proximity Read

[Analysis of a child with Osteo-oto-hepato-enteric syndrome and a literature review].Semantic proximity Read

[Zellweger syndrome caused by PEX6 gene variation in 2 cases and literature review].Semantic proximity Read

RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysis.Semantic proximity Read

Fifty years of recognizable patterns of human malformation: Insights and opportunities.Semantic proximity Read