Eating disorder - A diagnosis of exclusion

In adolescents with weight loss, diagnoses other than eating disorders should be considered, namely neurological diseases. A 16-year-old girl with an intellectual development disorder was referred to the Adolescent Medicine outpatient clinic from Child Psychiatry with a diagnosis of eating disorder and persistent anemia. Her body mass index was consistently below the fifth percentile and long-lasting eating difficulties were reported since the age of 15. The girl had no other gastrointestinal, articular, or respiratory complaints, neither polyuria, polydipsia, or recurrent fever. Parental divorce and domestic violence were reported. The patient complained of excessive daytime sleepiness, asthenia, intermittent myalgia, and muscular weakness episodes. Phenotypic characteristics and personal medical history led to clinical suspicion of a neuromuscular disease and genetic study confirmed myotonic dystrophy type 1. This case highlights the importance of considering other diagnoses besides eating disorders in adolescents with eating problems. An exhaustive evaluation of personal and family medical history, patient complaints, and detailed physical examination is mandatory.

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Main Authors: Fonseca,Margarida Silva, Santos,Helena, Guedes,Raquel, Tavares,Hugo Braga
Format: Digital revista
Language:English
Published: Centro Hospitalar do Porto 2020
Online Access:http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-07542020000200007
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spelling oai:scielo:S0872-075420200002000072021-02-17Eating disorder - A diagnosis of exclusionFonseca,Margarida SilvaSantos,HelenaGuedes,RaquelTavares,Hugo Braga adolescence eating disorders genetic testing myotonic dystrophy type 1 In adolescents with weight loss, diagnoses other than eating disorders should be considered, namely neurological diseases. A 16-year-old girl with an intellectual development disorder was referred to the Adolescent Medicine outpatient clinic from Child Psychiatry with a diagnosis of eating disorder and persistent anemia. Her body mass index was consistently below the fifth percentile and long-lasting eating difficulties were reported since the age of 15. The girl had no other gastrointestinal, articular, or respiratory complaints, neither polyuria, polydipsia, or recurrent fever. Parental divorce and domestic violence were reported. The patient complained of excessive daytime sleepiness, asthenia, intermittent myalgia, and muscular weakness episodes. Phenotypic characteristics and personal medical history led to clinical suspicion of a neuromuscular disease and genetic study confirmed myotonic dystrophy type 1. This case highlights the importance of considering other diagnoses besides eating disorders in adolescents with eating problems. An exhaustive evaluation of personal and family medical history, patient complaints, and detailed physical examination is mandatory.info:eu-repo/semantics/openAccessCentro Hospitalar do PortoNascer e Crescer v.29 n.2 20202020-06-01info:eu-repo/semantics/reporttext/htmlhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-07542020000200007en10.25753/BirthGrowthMJ.v29.i2.15091
institution SCIELO
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country Portugal
countrycode PT
component Revista
access En linea
databasecode rev-scielo-pt
tag revista
region Europa del Sur
libraryname SciELO
language English
format Digital
author Fonseca,Margarida Silva
Santos,Helena
Guedes,Raquel
Tavares,Hugo Braga
spellingShingle Fonseca,Margarida Silva
Santos,Helena
Guedes,Raquel
Tavares,Hugo Braga
Eating disorder - A diagnosis of exclusion
author_facet Fonseca,Margarida Silva
Santos,Helena
Guedes,Raquel
Tavares,Hugo Braga
author_sort Fonseca,Margarida Silva
title Eating disorder - A diagnosis of exclusion
title_short Eating disorder - A diagnosis of exclusion
title_full Eating disorder - A diagnosis of exclusion
title_fullStr Eating disorder - A diagnosis of exclusion
title_full_unstemmed Eating disorder - A diagnosis of exclusion
title_sort eating disorder - a diagnosis of exclusion
description In adolescents with weight loss, diagnoses other than eating disorders should be considered, namely neurological diseases. A 16-year-old girl with an intellectual development disorder was referred to the Adolescent Medicine outpatient clinic from Child Psychiatry with a diagnosis of eating disorder and persistent anemia. Her body mass index was consistently below the fifth percentile and long-lasting eating difficulties were reported since the age of 15. The girl had no other gastrointestinal, articular, or respiratory complaints, neither polyuria, polydipsia, or recurrent fever. Parental divorce and domestic violence were reported. The patient complained of excessive daytime sleepiness, asthenia, intermittent myalgia, and muscular weakness episodes. Phenotypic characteristics and personal medical history led to clinical suspicion of a neuromuscular disease and genetic study confirmed myotonic dystrophy type 1. This case highlights the importance of considering other diagnoses besides eating disorders in adolescents with eating problems. An exhaustive evaluation of personal and family medical history, patient complaints, and detailed physical examination is mandatory.
publisher Centro Hospitalar do Porto
publishDate 2020
url http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-07542020000200007
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AT santoshelena eatingdisorderadiagnosisofexclusion
AT guedesraquel eatingdisorderadiagnosisofexclusion
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