Cargando…

Type III Mixed Cryoglobulinemia and Antiphospholipid Syndrome in a Patient With Partial DiGeorge Syndrome

We studied a 14 year-old boy with partial DiGeorge syndrome (DGS), status post complete repair of Tetralogy of Fallot, who developed antiphospholipid syndrome (APS) and type III mixed cryoglobulinemia. He presented with recurrent fever and dyspnea upon exertion secondary to right pulmonary embolus o...

Descripción completa

Detalles Bibliográficos
Autores principales:	Chang, Alice D., Tachdjian, Raffi, Gallagher, Kerry, McCurdy, Deborah K., Lassman, Charles, Stiehm, E. Richard, Yadin, Ora
Formato:	Texto
Lenguaje:	English
Publicado:	Hindawi Publishing Corporation 2006
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2270767/ https://www.ncbi.nlm.nih.gov/pubmed/17162366 http://dx.doi.org/10.1080/17402520600877778

Ejemplares similares

Clinical Phenotype of DiGeorge Syndrome with Negative Genetic Tests: A Case of DiGeorge-Like Syndrome?
por: Laccetta, Gianluigi, et al.
Publicado: (2015)

Follicular Helper T Cells in DiGeorge Syndrome
por: Klocperk, Adam, et al.
Publicado: (2018)

DiGeorge Syndrome with Sacral Myelomeningocele and Epilepsy
por: Alkan, Gülsüm, et al.
Publicado: (2017)

DiGeorge’s syndrome presenting as hypocalcemia in an adult
por: Aljabri, K.S., et al.
Publicado: (2005)

Craniofacial Phenotypes and Genetics of DiGeorge Syndrome
por: Funato, Noriko
Publicado: (2022)

Psychiatric Comorbidities in Adults with DiGeorge Syndrome
por: Patel, Hiren, et al.
Publicado: (2022)

DiGeorge Syndrome: a not so rare disease
por: Fomin, Angela BF, et al.
Publicado: (2010)

Infectious Complications of DiGeorge Syndrome in the Setting of Malignancy
por: Hare, Heather, et al.
Publicado: (2022)

A young man with DiGeorge syndrome and tachycardia
por: Bradt, Nicolas, et al.
Publicado: (2023)

A young man with DiGeorge syndrome and tachycardia
por: Bradt, Nicolas, et al.
Publicado: (2023)

Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci
por: Morcel, Karine, et al.
Publicado: (2011)

DiGeorge syndrome presenting as late onset hypocalcaemia in adulthood
por: Johnston, Philip C, et al.
Publicado: (2008)

DiGeorge Syndrome Presenting as Hypocalcaemia-Induced Seizures in Adulthood
por: Zammit, Adrian, et al.
Publicado: (2013)

Revision Surgery in Permanent Patellar Dislocation in DiGeorge Syndrome
por: Berruto, Massimo, et al.
Publicado: (2015)

DiGeorge syndrome who developed lymphoproliferative mediastinal mass
por: Kim, Kyu Yeun, et al.
Publicado: (2015)

“FISHed” out the diagnosis: A case of DiGeorge syndrome
por: Bajaj, S, et al.
Publicado: (2016)

Thymus transplantation for complete DiGeorge syndrome: European experience
por: Davies, E. Graham, et al.
Publicado: (2017)

Schizophrenia in DiGeorge Syndrome: A Unique Case Report
por: Rizvi, Sukaina, et al.
Publicado: (2018)

Clozapine-induced myocarditis in an adolescent male with DiGeorge Syndrome
por: Ruhe, Ann Marie, et al.
Publicado: (2018)

DiGeorge Syndrome and COVID-19 in Two Pediatric Patients
por: Fallatah, Eilaf, et al.
Publicado: (2021)

Camptodactyly and DiGeorge syndrome: A rare hand anomaly
por: Hurley, C.M., et al.
Publicado: (2021)

Neuroinflammation and Oxidative Stress in Individuals Affected by DiGeorge Syndrome
por: Menghi, Michela, et al.
Publicado: (2023)

DiGeorge Syndrome With Absence of Speech: A Rare Case
por: Jayaprakasan, Srilakshmi K, et al.
Publicado: (2023)

MOZ Regulates the Tbx1 Locus, and Moz Mutation Partially Phenocopies DiGeorge Syndrome
por: Voss, Anne K., et al.
Publicado: (2012)

Aspiration pneumonia in the child with DiGeorge syndrome -A case report-
por: Lee, Ji-Young, et al.
Publicado: (2011)

Immunodeficiency in DiGeorge Syndrome and Options for Treating Cases with Complete Athymia
por: Davies, E. Graham
Publicado: (2013)

The TREC/KREC Assay for the Diagnosis and Monitoring of Patients with DiGeorge Syndrome
por: Froňková, Eva, et al.
Publicado: (2014)

An exploratory study of predisposing genetic factors for DiGeorge/velocardiofacial syndrome
por: Vergés, Laia, et al.
Publicado: (2017)

DiGeorge syndrome: Relevance of psychiatric symptoms in undiagnosed adult patients
por: Kraus, Christoph, et al.
Publicado: (2018)

Wandering spleen with splenic torsion in a child with DiGeorge syndrome
por: Taylor, Charlotte S., et al.
Publicado: (2019)

Case Report: Two Patients with Partial DiGeorge Syndrome Presenting with Attention Disorder and Learning Difficulties
por: Hacıhamdioğlu, Bülent, et al.
Publicado: (2011)

Case report: Effectiveness of sirolimus in treating partial DiGeorge Syndrome with Autoimmune Lymphoproliferative Syndrome (ALPS)-like features
por: Gu, Hao, et al.
Publicado: (2023)

Diversification, not use, of the immunoglobulin VH gene repertoire is restricted in DiGeorge syndrome
Publicado: (1993)

The evaluation of DiGeorge syndrome gene deletion using molecular cytogenetic techniques
por: Bahamat, Abeer A, et al.
Publicado: (2014)

Cardiovascular Malformations in CHARGE Syndrome with DiGeorge Phenotype: Two Case Reports
por: Yasuda, Kazushi, et al.
Publicado: (2016)

Early-onset psychosis in an adolescent with DiGeorge syndrome: A case report
por: Molebatsi, Keneilwe, et al.
Publicado: (2018)

An Unexplained Case of Progressive Spastic Paraparesis in an Individual with Known DiGeorge Syndrome
por: Dhoot, Roshni, et al.
Publicado: (2020)

Ruptured Sinus of Valsalva Aneurysm Mimicking Infective Endocarditis in DiGeorge Syndrome
por: Bhimani, Salima A., et al.
Publicado: (2019)

Metabolic Parameters in Patients with Prader-Willi Syndrome and DiGeorge Syndrome with Respect to Psychopathological Manifestation
por: Krefft, Maja, et al.
Publicado: (2020)

Case report of 5 siblings: malnutrition? Rickets? DiGeorge syndrome? Developmental delay?
por: Cundiff, David K, et al.
Publicado: (2006)

Cannot write session to /tmp/vufind_sessions/sess_kh1kjka9hre58ertdeh78ab5tr