Onset of psychiatric signs and impaired neurocognitive domains in inherited metabolic disorders: A case series

Abstract Inherited metabolic disorders (IMDs) can present with psychiatric signs that vary widely from one disease to another. This picture is further complicated by the fact that these features occur at very different illness time points, which may further delay appropriate diagnosis and treatment....

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Main Authors: François Medjkane, Marine Bohet, Marielle Ister, David Cohen, Aesa Parenti, Majda Janati, Karine Mention, Dries Dobbelaere, Renaud Jardri
Format: Article
Language:English
Published: Wiley 2021-03-01
Series:JIMD Reports
Subjects:
DSM
Online Access:https://doi.org/10.1002/jmd2.12133
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spelling doaj-0d851fda86d045b89d8dcfe26bc50e262021-03-05T02:17:51ZengWileyJIMD Reports2192-83122021-03-01581293610.1002/jmd2.12133Onset of psychiatric signs and impaired neurocognitive domains in inherited metabolic disorders: A case seriesFrançois Medjkane0Marine Bohet1Marielle Ister2David Cohen3Aesa Parenti4Majda Janati5Karine Mention6Dries Dobbelaere7Renaud Jardri8CHU Lille Service de Psychiatrie Enfants et Adolescents, Centre de Référence des Maladies Rares à Expression Psychiatrique, Hôpital Fontan Lille FranceCHU Lille Service de Psychiatrie Enfants et Adolescents, Centre de Référence des Maladies Rares à Expression Psychiatrique, Hôpital Fontan Lille FranceService de Pédiatrie Hôpital Victor Provo Roubaix FranceDépartement de Psychiatrie Enfants et Adolescents AP‐HP, GH Pitié‐Salpêtrière Paris FranceCHU Lille Service de Psychiatrie Enfants et Adolescents, Centre de Référence des Maladies Rares à Expression Psychiatrique, Hôpital Fontan Lille FranceCHU Lille Service de Psychiatrie Enfants et Adolescents, Centre de Référence des Maladies Rares à Expression Psychiatrique, Hôpital Fontan Lille FranceReference Centre for Inherited Metabolic Diseases in Child and Adulthood, University Children's Hospital Jeanne de Flandre and RADEME Lille Cedex FranceReference Centre for Inherited Metabolic Diseases in Child and Adulthood, University Children's Hospital Jeanne de Flandre and RADEME Lille Cedex FranceCHU Lille Service de Psychiatrie Enfants et Adolescents, Centre de Référence des Maladies Rares à Expression Psychiatrique, Hôpital Fontan Lille FranceAbstract Inherited metabolic disorders (IMDs) can present with psychiatric signs that vary widely from one disease to another. This picture is further complicated by the fact that these features occur at very different illness time points, which may further delay appropriate diagnosis and treatment. In this case series of 62 children and adolescents suffering from IMDs, we clustered psychiatric signs (on the basis of the fifth edition of the Diagnostic and Statistical Manual for Mental Disorders classification) as well as impaired cognitive domains (on the basis of the Research Domain Criteriamatrix) according to their mean age of onset (5.7 ± 4 years). We observed consistent patterns of occurrence across disorders. Externalizing symptoms, sleep problems, and cross‐domain self‐regulation deficits were found to precede the IMD diagnosis. Repetitive thoughts and behaviors as well as emotional dysregulation were found to occur around the disease onset. Finally, late‐onset features included dissociative or eating disorders, together with impaired emotion knowledge. Clinicians should specifically look for the co‐occurrence of age‐specific atypical signs, such as treatment resistance or worsening with psychotropic medication in the earliest stages and symptom fluctuation, confusion, catatonia, or isolated visual hallucinations. We believe that the combined characterizations of psychiatric signs and impaired neurocognitive domains may enable the earliest detection of IMDs and the appropriate care of these particular manifestations. Key Points Psychiatric signs are common in inherited metabolic disorders (IMDs) and may occur in the same age‐range as other clinical manifestations. Three clusters of psychiatric signs and two clusters of neurocognitive domains can be defined according to their mean age of onset. Warning signs to be used in liaison psychiatry should include age‐specific cognitive impairmentshttps://doi.org/10.1002/jmd2.12133cognitiondevelopmentDSMpsychiatryrare diseaseRDoC
collection DOAJ
language English
format Article
sources DOAJ
author François Medjkane
Marine Bohet
Marielle Ister
David Cohen
Aesa Parenti
Majda Janati
Karine Mention
Dries Dobbelaere
Renaud Jardri
spellingShingle François Medjkane
Marine Bohet
Marielle Ister
David Cohen
Aesa Parenti
Majda Janati
Karine Mention
Dries Dobbelaere
Renaud Jardri
Onset of psychiatric signs and impaired neurocognitive domains in inherited metabolic disorders: A case series
JIMD Reports
cognition
development
DSM
psychiatry
rare disease
RDoC
author_facet François Medjkane
Marine Bohet
Marielle Ister
David Cohen
Aesa Parenti
Majda Janati
Karine Mention
Dries Dobbelaere
Renaud Jardri
author_sort François Medjkane
title Onset of psychiatric signs and impaired neurocognitive domains in inherited metabolic disorders: A case series
title_short Onset of psychiatric signs and impaired neurocognitive domains in inherited metabolic disorders: A case series
title_full Onset of psychiatric signs and impaired neurocognitive domains in inherited metabolic disorders: A case series
title_fullStr Onset of psychiatric signs and impaired neurocognitive domains in inherited metabolic disorders: A case series
title_full_unstemmed Onset of psychiatric signs and impaired neurocognitive domains in inherited metabolic disorders: A case series
title_sort onset of psychiatric signs and impaired neurocognitive domains in inherited metabolic disorders: a case series
publisher Wiley
series JIMD Reports
issn 2192-8312
publishDate 2021-03-01
description Abstract Inherited metabolic disorders (IMDs) can present with psychiatric signs that vary widely from one disease to another. This picture is further complicated by the fact that these features occur at very different illness time points, which may further delay appropriate diagnosis and treatment. In this case series of 62 children and adolescents suffering from IMDs, we clustered psychiatric signs (on the basis of the fifth edition of the Diagnostic and Statistical Manual for Mental Disorders classification) as well as impaired cognitive domains (on the basis of the Research Domain Criteriamatrix) according to their mean age of onset (5.7 ± 4 years). We observed consistent patterns of occurrence across disorders. Externalizing symptoms, sleep problems, and cross‐domain self‐regulation deficits were found to precede the IMD diagnosis. Repetitive thoughts and behaviors as well as emotional dysregulation were found to occur around the disease onset. Finally, late‐onset features included dissociative or eating disorders, together with impaired emotion knowledge. Clinicians should specifically look for the co‐occurrence of age‐specific atypical signs, such as treatment resistance or worsening with psychotropic medication in the earliest stages and symptom fluctuation, confusion, catatonia, or isolated visual hallucinations. We believe that the combined characterizations of psychiatric signs and impaired neurocognitive domains may enable the earliest detection of IMDs and the appropriate care of these particular manifestations. Key Points Psychiatric signs are common in inherited metabolic disorders (IMDs) and may occur in the same age‐range as other clinical manifestations. Three clusters of psychiatric signs and two clusters of neurocognitive domains can be defined according to their mean age of onset. Warning signs to be used in liaison psychiatry should include age‐specific cognitive impairments
topic cognition
development
DSM
psychiatry
rare disease
RDoC
url https://doi.org/10.1002/jmd2.12133
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