Cargando…

Endocrine Disorders and Genital Infections Impair Gynecological Health in APECED (APS-1)

OBJECTIVE: In autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) defects in the autoimmune regulator gene lead to impaired immunotolerance. We explored the effects of immunodeficiency and endocrinopathies on gynecologic health in patients with APECED. DESIGN: Cross-sectional coh...

Descripción completa

Detalles Bibliográficos
Autores principales:	Saari, Viivi, Laakso, Saila, Tiitinen, Aila, Mäkitie, Outi, Holopainen, Elina
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Endocrinology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8669951/ https://www.ncbi.nlm.nih.gov/pubmed/34917035 http://dx.doi.org/10.3389/fendo.2021.784195

Ejemplares similares

Severe Phenotype of APECED (APS1) Increases Risk for Structural Bone Alterations
por: Laakso, Saila, et al.
Publicado: (2020)

Pregnancy Outcome in Women With APECED (APS-1): A Multicenter Study on 43 Females With 83 Pregnancies
por: Laakso, Saila, et al.
Publicado: (2021)

Recurrent Hypokalemia and Adrenal Steroids in Patients With APECED
por: Borchers, Joonatan, et al.
Publicado: (2022)

Patients With APECED Have Increased Early Mortality Due to Endocrine Causes, Malignancies and infections
por: Borchers, Joonatan, et al.
Publicado: (2020)

Gynecologic assessment of 19 adult females with cartilage-hair hypoplasia – high rate of HPV positivity
por: Holopainen, Elina, et al.
Publicado: (2018)

Fecal Bacteria Implicated in Biofilm Production Are Enriched and Associate to Gastrointestinal Symptoms in Patients With APECED – A Pilot Study
por: Hetemäki, Iivo, et al.
Publicado: (2021)

Oral Tongue Malignancies in Autoimmune Polyendocrine Syndrome Type 1
por: Bruserud, Øyvind, et al.
Publicado: (2018)

Epidemiology and Causes of Primary Adrenal Insufficiency in Children: A Population-Based Study
por: Borchers, Joonatan, et al.
Publicado: (2023)

Outcomes of 42 pregnancies in 14 women with cartilage-hair hypoplasia: a retrospective cohort study
por: Holopainen, Elina, et al.
Publicado: (2020)

Generation and Characterization of iPS Cells Derived from APECED Patients for Gene Correction
por: Karvonen, Eira, et al.
Publicado: (2022)

A Novel Osteochondrodysplasia With Empty Sella Associates With a TBX2 Variant
por: Mäkitie, Riikka E., et al.
Publicado: (2022)

Craniofacial and Craniocervical Features in Cartilage-Hair Hypoplasia: A Radiological Study of 17 Patients and 34 Controls
por: Arponen, Heidi, et al.
Publicado: (2021)

Copeptin analysis in endocrine disorders
por: Moodley, Nareshni
Publicado: (2023)

Endocrine Disruptor Compounds—A Cause of Impaired Immune Tolerance Driving Inflammatory Disorders of Pregnancy?
por: Schjenken, John E., et al.
Publicado: (2021)

New Insights Into Monogenic Causes of Osteoporosis
por: Mäkitie, Riikka E., et al.
Publicado: (2019)

Lipocalin-2 is associated with FGF23 in WNT1 and PLS3 osteoporosis
por: Loid, Petra, et al.
Publicado: (2022)

Quantification of urinary total luteinizing hormone immunoreactivity may improve the prediction of ovulation time
por: Demir, And, et al.
Publicado: (2022)

Patients with autoimmune polyendocrine syndrome type 1 have an increased susceptibility to severe herpesvirus infections
por: Hetemäki, Iivo, et al.
Publicado: (2021)

Editorial: Omics Solutions for Endocrine Disorders
por: Atkin, Stephen L., et al.
Publicado: (2022)

Endocrine disorders and fertility and pregnancy: An update
por: Bendarska-Czerwińska, Anna, et al.
Publicado: (2023)

Editorial: Endothelial dysfunction in endocrine disorders
por: Radenković, Miroslav, et al.
Publicado: (2023)

Editorial: Estrogen receptors in endocrine disorders
por: Filardi, Tiziana, et al.
Publicado: (2023)

Editorial: Endocrine consequences of sleep disorders
por: Uchima Koecklin, Karin Harumi, et al.
Publicado: (2023)

Editorial: Osteoporosis secondary to endocrine disorders
por: Skowrońska-Jóźwiak, Elżbieta, et al.
Publicado: (2023)

Gonadal Failure Is Common in Long-Term Survivors of Childhood High-Risk Neuroblastoma Treated With High-Dose Chemotherapy and Autologous Stem Cell Rescue
por: Utriainen, Pauliina, et al.
Publicado: (2019)

SGMS2 in primary osteoporosis with facial nerve palsy
por: Pihlström, Sandra, et al.
Publicado: (2023)

Editorial: Neurological and Psychiatric Disorders in Endocrine Diseases
por: Tamagno, Gianluca, et al.
Publicado: (2015)

Metabolism and Endocrine Disorders: What Wnt Wrong?
por: Franco, Carolina N., et al.
Publicado: (2022)

SIRT1 and Autophagy: Implications in Endocrine Disorders
por: Kim, Ji Yong, et al.
Publicado: (2022)

Editorial: Wnt signaling in endocrine and metabolic disorders
por: Cailotto, Frederic, et al.
Publicado: (2023)

Polyostotic Fibrous Dysplasia With and Without McCune–Albright Syndrome—Clinical Features in a Nordic Pediatric Cohort
por: Utriainen, Pauliina, et al.
Publicado: (2018)

SAT-241 Hyposplenism and Autoimmune Hepatitis: Rare Complications of Autoimmune Polyendocrinopathy Candidiasis and Ectodermal Dystrophy (APECED)
por: Miller, Clare, et al.
Publicado: (2019)

Corrigendum: “Editorial: Neurological and Psychiatric Disorders in Endocrine Diseases”
por: Tamagno, Gianluca, et al.
Publicado: (2015)

The Emerging Roles of Endocrine Hormones in Different Arthritic Disorders
por: Bertoldo, Eugenia, et al.
Publicado: (2021)

Editorial: Placental Hormones and Pregnancy-Related Endocrine Disorders
por: Zhou, Qiongjie, et al.
Publicado: (2022)

PLS3 Mutations Cause Severe Age and Sex-Related Spinal Pathology
por: Mäkitie, Riikka E., et al.
Publicado: (2020)

Long-term Outcome of Kidney Transplantation in 6 Patients With Autoimmune Polyendocrinopathy-candidiasis-ectodermal Dystrophy
por: Laakso, Saila, et al.
Publicado: (2021)

SAT-216 Prevalence of Endocrine, Gynecological and Other Medical Conditions Among Adult Women with Turner Syndrome
por: Farquhar, Madeleine, et al.
Publicado: (2019)

Rare Variants in Genes Linked to Appetite Control and Hypothalamic Development in Early-Onset Severe Obesity
por: Loid, Petra, et al.
Publicado: (2020)

Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility
por: Costantini, Alice, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_gv01munrb1iuivgfct4di1miad