Cargando…

Psychiatric Comorbidities in 1p36 Deletion Syndrome and Their Treatment—A Case Report

1p36 deletion syndrome represents the most common terminal deletion observed in humans. Major clinical findings comprise developmental delay/intellectual disability, poor or absent expressive language, congenital central muscular hypotonia, brain anomalies, brachydactyly/camptodactyly, short feet, a...

Descripción completa

Detalles Bibliográficos
Autor principal:	Briegel, Wolfgang
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2021
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8619815/ https://www.ncbi.nlm.nih.gov/pubmed/34831818 http://dx.doi.org/10.3390/ijerph182212064

Ejemplares similares

Psychiatric Disorders and Distal 21q Deletion—A Case Report
por: Briegel, Wolfgang, et al.
Publicado: (2020)

Deletion in 1p36.33-p36.32 is associated with pancytopenia: a case report
por: Yang, Huanhuan, et al.
Publicado: (2023)

1p36 deletion syndrome: first case report in Morocco detected by fluorescence in situ hybridization
por: Dafir, Kenza, et al.
Publicado: (2020)

Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review
por: Yokoyama, Emiy, et al.
Publicado: (2020)

A Novel Case of Biliary Atresia in a Premature Neonate With 1p36 Deletion Syndrome
por: Chawla, Vonita, et al.
Publicado: (2018)

Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case report
por: Nistico’, D., et al.
Publicado: (2020)

Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome
por: Toshimitsu, Masatake, et al.
Publicado: (2019)

1p36 deletion syndrome: an update
por: Jordan, Valerie K, et al.
Publicado: (2015)

Novel Point Mutation of EBSS Gene Coexisted with 1p36 Deletion
por: Zheng, Yue, et al.
Publicado: (2021)

1p36 deletion syndrome confirmed by fluorescence in situ hybridization and array-comparative genomic hybridization analysis
por: Kang, Dong Soo, et al.
Publicado: (2016)

Diagnosis and Treatment of Psychiatric Comorbidity in a Patient with Charles Bonnet Syndrome
por: Chen, Jasper J.
Publicado: (2014)

A rare cardiac phenotype of dextrocardia observed in a fetus with 1p36 deletion syndrome and a balanced translocation: a prenatal case report
por: Gao, Li, et al.
Publicado: (2020)

Familial deletion 18p syndrome: case report
por: Maranda, Bruno, et al.
Publicado: (2006)

Clinical Usefulness of Aripiprazole Treatment in a Girl with Prader-Willi Syndrome and Psychosis
por: Briegel, Wolfgang
Publicado: (2018)

Various Psychiatric Manifestation in DiGeorge Syndrome (22q11.2 Deletion Syndrome): A Case Report
por: Kim, Giok, et al.
Publicado: (2020)

1p36 Deletion Syndrome and Left Ventricular Non-compaction Cardiomyopathy—Two Cases Report
por: Jang, Subin, et al.
Publicado: (2021)

18p Deletion Syndrome: Case Report with Clinical Consideration and Management
por: Goyal, Megha, et al.
Publicado: (2017)

Patient With Delayed Development Resulting From De Novo Duplication of 7q36.1-q36.3 and Deletion of 9p24.3
por: Choi, Asayeon, et al.
Publicado: (2017)

Case report of individual with cutaneous immunodeficiency and novel 1p36 duplication
por: Hatter, Alyn D, et al.
Publicado: (2016)

Treatment of 22q11.2 deletion syndrome-associated schizophrenia with comorbid anxiety and panic disorder
por: Borders, Candace B., et al.
Publicado: (2017)

7q36 deletion and 9p22 duplication: effects of a double imbalance
por: Pelegrino, Karla de Oliveira, et al.
Publicado: (2013)

Detection of 1p36 deletion by clinical exome-first diagnostic approach
por: Watanabe, Miki, et al.
Publicado: (2016)

Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype
por: Stagi, Stefano, et al.
Publicado: (2014)

Aripiprazole treatment of Asperger’s syndrome in the acute psychiatric setting: case report
por: Dratcu, Luiz, et al.
Publicado: (2007)

The general anesthesia experience of deletion 8p syndrome patient -A case report-
por: Shin, Woo Jong, et al.
Publicado: (2011)

Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay
por: Seo, Go Hun, et al.
Publicado: (2016)

4q27 deletion and 7q36.1 microduplication in a patient with multiple malformations and hearing loss: a case report
por: Wu, Maolan, et al.
Publicado: (2020)

A case of 18p deletion syndrome after blepharoplasty
por: Xu, Li-juan, et al.
Publicado: (2017)

Adult ADHD: Questioning Diagnosis and Treatment in a Patient with Multiple Psychiatric Comorbidities
por: Chu, Robert Karoly, et al.
Publicado: (2017)

1p36 Deletion Syndrome and the Aorta: A Report of Three New Patients and a Literature Review
por: Lodato, Valentina, et al.
Publicado: (2021)

Psychiatric comorbidity in epilepsy and difficulties in treatment: A case report
por: Fernández Fariña, M., et al.
Publicado: (2022)

Chromosome 1p31.1 Deletion Syndrome: Limited Expression
por: Biswal, Seba, et al.
Publicado: (2021)

Cognitive Impairment in Inpatients with Prurigo Nodularis and Psychiatric Comorbidities
por: Lanza, Giuseppe, et al.
Publicado: (2021)

A case of de novo 18p deletion syndrome with panhypopituitarism
por: Yang, Aram, et al.
Publicado: (2019)

Psychological Adjustment of Children and Adolescents with 22q11.2 Deletion Syndrome and Their Mothers’ Stress and Coping—A Longitudinal Study
por: Briegel, Wolfgang, et al.
Publicado: (2021)

Psychiatric comorbidities in a young man with subacute myelopathy induced by abusive nitrous oxide consumption: a case report
por: Mancke, Falk, et al.
Publicado: (2016)

SAT139 Non-insulinoma Pancreatogenous Hypoglycemia Syndrome In A Patient With 1p36 Deletion Syndrome
por: Auckley, Elizabeth Diane, et al.
Publicado: (2023)

Obstacles to diagnostic investigation of a child with comorbid psychiatric conditions
por: Salem, Jena, et al.
Publicado: (2021)

Neuropathology of brain and spinal malformations in a case of monosomy 1p36
por: Shiba, Naoko, et al.
Publicado: (2013)

Deletion 21q22.3 and duplication 7q35q36.3 in a Colombian girl: a case report
por: Ruiz-Botero, Felipe, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_cv3ckudedgh7blag86bim6uj2u