Cargando…

Delirium with delayed diagnosis of hereditary coproporphyria

We present a hereditary coproporphyria patient with acute psychiatric symptoms and skin lesions initially misdiagnosed with schizoaffective disorder and later developed hyperactive delirium and atrial fibrillation requiring intensive care unit admission. He recovered after administering glucose infu...

Descripción completa

Detalles Bibliográficos
Autores principales:	Eroglu, Seyma, Birsenogul, Ilhan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Case Reports
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163461/ https://www.ncbi.nlm.nih.gov/pubmed/35662770 http://dx.doi.org/10.1002/ccr3.5937

Ejemplares similares

Hereditary coproporphyria.
por: Paterson, A., et al.
Publicado: (1994)

Neuropathic pain in hereditary coproporphyria
por: Chen, Guan-Liang, et al.
Publicado: (2013)

High penetrance, recurrent attacks and thrombus formation in a family with hereditary coproporphyria
por: Towns, Cindy, et al.
Publicado: (2022)

A Unique Neuropsychiatric Syndrome in Variant Hereditary Coproporphyria: Case Report and Review of the Literature
por: Baumgartner, Alex, et al.
Publicado: (2017)

Successful Radiation Therapy for Breast Cancer in a Patient With Hereditary Coproporphyria
por: Pennix, Thomas, et al.
Publicado: (2020)

P01-026 – A case of FMF and hereditary coproporphyria
por: Ganesha, A, et al.
Publicado: (2013)

Hereditary Coproporphyria Associated with the Q306X Mutation in the Coproporphyrin Oxidase Gene Presenting with Acute Ataxia
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2013)

A mouse model of hereditary coproporphyria identified in an ENU mutagenesis screen
por: Conway, Ashlee J., et al.
Publicado: (2017)

Hereditary Coproporphyria Mimicking Guillain-Barré Syndrome After COVID-19 Infection
por: Upchurch, Margaret, et al.
Publicado: (2022)

BALB.NCT-Cpox(nct) is a unique mouse model of hereditary coproporphyria
por: Kang, Xiaojing, et al.
Publicado: (2023)

Systemic Lupus Erythematosus and Hereditary Coproporphyria: Two Different Entities Diagnosed by WES in the Same Patient
por: Liu, Anlei, et al.
Publicado: (2022)

Cerebral Hypoperfusion in Hereditary Coproporphyria (HCP): A Single Photon Emission Computed Tomography (SPECT) Study
por: Valle, Guido, et al.
Publicado: (2016)

Greater disease burden of variegate porphyria than hereditary coproporphyria: An Israeli nationwide study of neurocutaneous porphyrias
por: Kaftory, Ran, et al.
Publicado: (2021)

A 25-Hour Fast Among Quiescent Hereditary Coproporphyria and Variegate Porphyria Patients is Associated With a Low Risk of Complications
por: Edel, Yonatan, et al.
Publicado: (2023)

Delayed Onset and Prolonged ECT-Related Delirium
por: Hassamal, Sameer, et al.
Publicado: (2013)

Albright hereditary osteodystrophy: Delay in the diagnosis of a rare disorder due to restricted medical services
por: Noor, Sahar, et al.
Publicado: (2023)

Hereditary spherocytosis: Consequences of delayed diagnosis
por: Steward, Sarah C, et al.
Publicado: (2014)

Pitfalls of delaying the diagnosis of hereditary haemorrhagic telangiectasia
por: Major, Tamás, et al.
Publicado: (2019)

Delayed diagnosis of traumatic diaphragmatic hernia may cause colonic perforation: a case report
por: Ozkan, Orhan Veli, et al.
Publicado: (2009)

Delayed Onset, Protracted Delirium and Aspiration Pneumonitis Associated with a Combination of Clozapine and Electroconvulsive Therapy
por: Manjunatha, N., et al.
Publicado: (2011)

The physician and hereditary angioedema friend or foe: 62-year diagnostic delay and iatrogenic procedures
por: Valerieva, Anna, et al.
Publicado: (2018)

588 Delayed Diagnosis of Hereditary Angioedema. A Case Report
por: González-Díaz, Sandra, et al.
Publicado: (2012)

Hereditary hemorrhagic telangiectasia of liver: Pathophysiology with role of radiology in diagnosis and treatment
por: Viyannan, Maheswaran, et al.
Publicado: (2020)

Prenatal diagnosis of hereditary diffuse gastric cancer: a case report
por: Xiao, Jun, et al.
Publicado: (2023)

Hereditary angioedema with C1 inhibitor deficiency: delay in diagnosis in Europe
por: Zanichelli, Andrea, et al.
Publicado: (2013)

Use of Phenobarbital in Delirium Tremens
por: Fujimoto, Jeffrey, et al.
Publicado: (2017)

Acute Delirium Associated With Levofloxacin
por: Kogan, Yana, et al.
Publicado: (2018)

Tramadol: Delirium: case report
Publicado: (2020)

Delirium After Pregabalin Withdrawal
por: Çalışkan, Ali Metehan, et al.
Publicado: (2021)

Diagnosis and treatment of hereditary hemorrhagic telangiectasia in a pediatric patient with chronic cyanosis
por: Johnson, BV, et al.
Publicado: (2016)

Complicated and delayed diagnosis of tuberculous peritonitis
por: Bolognesi, Massimo, et al.
Publicado: (2013)

Eosinophilic Enteritis: A Delayed Diagnosis
por: Munjal, Ankita, et al.
Publicado: (2017)

Delayed discharge and frailty, delirium and functional decline
por: Heckman, George A., et al.
Publicado: (2021)

Delayed diagnosis of severe tuberculous spondylodiscitis in an asylum seeker; patient or doctors delay?
por: Kristensen, Kristina Langholz, et al.
Publicado: (2017)

Acute Delirium due to Parenteral Tramadol
por: Ghosh, Soumitra, et al.
Publicado: (2013)

Takotsubo cardiomyopathy precipitated by delirium tremens
por: Agu, Chidozie Charles, et al.
Publicado: (2015)

Delirium, Caused by Suspending Treatment of Hypothyroidism
por: Hernández-Sandí, Alejandro, et al.
Publicado: (2016)

Levomepromazine: Delirium and sedation: case report
Publicado: (2021)

Haloperidol/quetiapine: Paradoxical worsening of delirium resulted in hypoactive delirium and unmasking of previously undiagnosed parkinsonism: case report
Publicado: (2020)

Recognized homonymous hemianopsia and delirium during the admission examination leading to diagnosis and appropriate treatment of a new stroke
por: Tsymbalov, Konstantin S, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_c4epti34t771rvku87moi8bfgq