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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Centro Hospitalar do Porto
2020
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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 |
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Fonseca,Margarida Silva Santos,Helena Guedes,Raquel Tavares,Hugo Braga |
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Fonseca,Margarida Silva Santos,Helena Guedes,Raquel Tavares,Hugo Braga Eating disorder - A diagnosis of exclusion |
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Fonseca,Margarida Silva Santos,Helena Guedes,Raquel Tavares,Hugo Braga |
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Fonseca,Margarida Silva |
title |
Eating disorder - A diagnosis of exclusion |
title_short |
Eating disorder - A diagnosis of exclusion |
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Eating disorder - A diagnosis of exclusion |
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Eating disorder - A diagnosis of exclusion |
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Eating disorder - A diagnosis of exclusion |
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eating disorder - a diagnosis of exclusion |
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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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Centro Hospitalar do Porto |
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2020 |
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http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-07542020000200007 |
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AT fonsecamargaridasilva eatingdisorderadiagnosisofexclusion AT santoshelena eatingdisorderadiagnosisofexclusion AT guedesraquel eatingdisorderadiagnosisofexclusion AT tavareshugobraga eatingdisorderadiagnosisofexclusion |
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1756001824214614016 |