Cargando…

Low circulating PCSK9 levels in LPL homozygous children with chylomicronemia syndrome in a syrian refugee family in Lebanon

Familial chylomicronemia syndrome is a rare autosomal recessive disorder of lipoprotein metabolism characterized by the presence of chylomicrons in fasting plasma and an important increase in plasma triglycerides (TG) levels that can exceed 22.58 mmol/l. The disease is associated with recurrent epis...

Descripción completa

Detalles Bibliográficos
Autores principales:	Ayoub, Carine, Azar, Yara, Maddah, Dina, Ghaleb, Youmna, Elbitar, Sandy, Abou-Khalil, Yara, Jambart, Selim, Varret, Mathilde, Boileau, Catherine, El Khoury, Petra, Abifadel, Marianne
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2022
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437297/ https://www.ncbi.nlm.nih.gov/pubmed/36061186 http://dx.doi.org/10.3389/fgene.2022.961028

Ejemplares similares

Circulating PCSK9 Linked to Dyslipidemia in Lebanese Schoolchildren
por: Azar, Yara, et al.
Publicado: (2022)

Identification of a Variant in APOB Gene as a Major Cause of Hypobetalipoproteinemia in Lebanese Families
por: Ayoub, Carine, et al.
Publicado: (2021)

New Sequencing technologies help revealing unexpected mutations in Autosomal Dominant Hypercholesterolemia
por: Elbitar, Sandy, et al.
Publicado: (2018)

Experts’ opinion on the detection and management of prediabetes in Lebanon
por: Andari, Emile, et al.
Publicado: (2021)

Whole Exome/Genome Sequencing Joint Analysis of a Family with Oligogenic Familial Hypercholesterolemia
por: Ghaleb, Youmna, et al.
Publicado: (2022)

Analysis of a Chinese Pedigree With Familial Chylomicronemia Syndrome Reveals Two Novel LPL Mutations by Whole-Exome Sequencing
por: Liu, Ying, et al.
Publicado: (2020)

Novel pathogenic variant combination in LPL causing familial chylomicronemia syndrome in an Asian family and experimental validation in vitro: a case report
por: Shi, Huiping, et al.
Publicado: (2022)

The Association Between the Syrian Crisis and Cutaneous Leishmaniasis in Lebanon
por: Bizri, Nazih A., et al.
Publicado: (2021)

Loss-of-Function Homozygous Variant in LPL Causes Type I Hyperlipoproteinemia and Renal Lipidosis
por: Wu, Hongyan, et al.
Publicado: (2023)

Factors influencing dyslipidemia in statin-treated patients in Lebanon and Jordan: results of the Dyslipidemia International Study
por: Azar, Sami T, et al.
Publicado: (2014)

Evaluation of a digital intervention for depression among Lebanese&Syrian refugees in Lebanon
por: Abi Ramia, J, et al.
Publicado: (2023)

Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm
por: Elbitar, Sandy, et al.
Publicado: (2020)

Homozygous LPL p.Gly188Glu Mutation in a Mexican Girl With Lipoprotein Lipase Deficiency
por: Colima Fausto, Ana Gabriela, et al.
Publicado: (2017)

An assessment of antenatal care among Syrian refugees in Lebanon
por: Benage, Matthew, et al.
Publicado: (2015)

Health system resilience: Lebanon and the Syrian refugee crisis
por: Ammar, Walid, et al.
Publicado: (2016)

Lebanon: mental health system reform and the Syrian crisis
por: Karam, Elie, et al.
Publicado: (2016)

Syrian refugees in Lebanon: the search for universal health coverage
por: Blanchet, Karl, et al.
Publicado: (2016)

The multidimensional burden of COVID-19 on Syrian refugees in Lebanon
por: Hajjar, Marwan S, et al.
Publicado: (2021)

Health equity of displaced Syrians in Lebanon: Riwa Khalifeh
por: Khalifeh, R, et al.
Publicado: (2022)

Dissection of Clinical and Gene Expression Signatures of Familial versus Multifactorial Chylomicronemia
por: Tremblay, Karine, et al.
Publicado: (2020)

Rare Treatments for Rare Dyslipidemias: New Perspectives in the Treatment of Homozygous Familial Hypercholesterolemia (HoFH) and Familial Chylomicronemia Syndrome (FCS)
por: D’Erasmo, Laura, et al.
Publicado: (2021)

Ongoing Epidemic of Cutaneous Leishmaniasis among Syrian Refugees, Lebanon
por: Saroufim, Maya, et al.
Publicado: (2014)

Dialysis therapy for Syrian refugees in Lebanon: a call for action
por: Karah, Nabil, et al.
Publicado: (2018)

Community-Based Noncommunicable Disease Care for Syrian Refugees in Lebanon
por: Sethi, Stephen, et al.
Publicado: (2017)

Vulnerability of Syrian refugees in Lebanon to COVID-19: quantitative insights
por: Fouad, Fouad M., et al.
Publicado: (2021)

Prevalence of Malnutrition among Syrian Refugee Children from Lebanon
por: Mroue, Tamara, et al.
Publicado: (2023)

A Comprehensive Update on the Chylomicronemia Syndrome
por: Goldberg, Ronald B., et al.
Publicado: (2020)

Current Diagnosis and Management of Primary Chylomicronemia
por: Okazaki, Hiroaki, et al.
Publicado: (2021)

The Evolving Story of Multifactorial Chylomicronemia Syndrome
por: Paquette, Martine, et al.
Publicado: (2022)

Multi-purpose cash transfers and health among vulnerable Syrian refugees in Lebanon: a prospective cohort study
por: Lyles, Emily, et al.
Publicado: (2021)

Assessment of the health needs of Syrian refugees in Lebanon and Syria’s neighboring countries
por: El Arnaout, Nour, et al.
Publicado: (2019)

Comments on the article: “Syrian refugees in Lebanon: the search for universal health coverage”
por: Ammar, Walid, et al.
Publicado: (2016)

Displacement, deprivation and hard work among Syrian refugee children in Lebanon
por: Habib, Rima R, et al.
Publicado: (2019)

Deletion of GPIHBP1 causing severe chylomicronemia
por: Rios, Jonathan J., et al.
Publicado: (2011)

Two Case Reports of Familial Chylomicronemia Syndrome
por: Chen, Yan-Hui, et al.
Publicado: (2012)

The burden of familial chylomicronemia syndrome in Canadian patients
por: Gaudet, Daniel, et al.
Publicado: (2020)

Familial chylomicronemia syndrome: a case report
por: Susheela, Ammu Thampi, et al.
Publicado: (2021)

Non-Alcoholic Fatty Liver in Patients with Chylomicronemia
por: Maltais, Mélanie, et al.
Publicado: (2021)

Familial chylomicronemia syndrome: importance of diagnostic vigilance
por: Ueda, Masako
Publicado: (2022)

Amelioration of Hypertriglyceridemia with Hypo-Alpha-Cholesterolemia in LPL Deficient Mice by Hematopoietic Cell-Derived LPL
por: Ding, Yinyuan, et al.
Publicado: (2011)

Cannot write session to /tmp/vufind_sessions/sess_25l26b9isr8kh21q079vqlvh5m