Cargando…

The coexistence of autoimmune diabetes and maturity-onset diabetes of the young (MODY): a case series

SUMMARY: The coexistence of autoimmune diabetes and maturity-onset diabetes (MODY) is rare. The absence of pancreatic autoantibodies is a key factor prompting MODY genetic testing. In this study, we report three cases of young-onset diabetes with progressive beta-cell dysfunction, strongly positive...

Descripción completa

Detalles Bibliográficos
Autores principales:	O’Donovan, Eimear Mary, Sanchez-Lechuga, Begona, Prehn, Emma, Byrne, Maria Michelle
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Bioscientifica Ltd 2022
Materias:	Insight into Disease Pathogenesis or Mechanism of Therapy
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9346313/ https://www.ncbi.nlm.nih.gov/pubmed/35894830 http://dx.doi.org/10.1530/EDM-21-0212

Ejemplares similares

A novel splice-site mutation of the HNF1B gene in a family with maturity onset diabetes of the young type 5 (MODY5)
por: Fujita, Yuki, et al.
Publicado: (2020)

Identification of a novel hepatocyte nuclear factor-1 alpha (HNF1A) variant in maturity onset diabetes of the young type 3 (HNF1A-MODY)
por: Verma, Megha, et al.
Publicado: (2022)

Combined treatment with sitagliptin and vitamin D in a patient with latent autoimmune diabetes in adults
por: Rapti, E, et al.
Publicado: (2016)

The onset of acute Charcot neuroarthropathy during pregnancy in patients with type 1 diabetes
por: Dardari, Dured, et al.
Publicado: (2020)

Pancreas-protective effect of rituximab for acute-onset type 1 diabetes in the honeymoon period: a case report
por: Kurozumi, Akira, et al.
Publicado: (2016)

A case of early-onset diabetes with impaired insulin secretion carrying a PAX6 gene Gln135* mutation
por: Sekiya, Motohiro, et al.
Publicado: (2022)

Diabetic ketoacidosis producing extreme hyperkalemia in a patient with type 1 diabetes on hemodialysis
por: Yamada, Hodaka, et al.
Publicado: (2017)

Transient diabetes insipidus in pregnancy
por: Marques, Pedro, et al.
Publicado: (2015)

Autoimmune polyendocrinopathy and hypophysitis after Puumala hantavirus infection
por: Tarvainen, Marlene, et al.
Publicado: (2016)

Fatty liver formation in fulminant type 1 diabetes
por: Matsuo, Takashi, et al.
Publicado: (2016)

Insulin Autoimmune Syndrome: a rare cause of postprandial hypoglycemia
por: Sahni, Pooja, et al.
Publicado: (2016)

Autoimmune alternating hyper- and hypo-thyroidism: a rare condition in pediatrics
por: Martins, Luísa Correia, et al.
Publicado: (2016)

Fructose-induced severe hypertriglyceridemia and diabetes mellitus: a cautionary tale
por: Dugic, Ana, et al.
Publicado: (2021)

Insulin autoimmune syndrome: not just one but two different diseases with therapeutic implications
por: Wammer, Anne Cathrine Parelius, et al.
Publicado: (2023)

Type B insulin resistance syndrome in a patient with type 1 diabetes
por: Sjöholm, Åke, et al.
Publicado: (2020)

Central diabetes insipidus and partial anterior pituitary dysfunction in acute myeloid leukemia
por: Arya, Rigya, et al.
Publicado: (2022)

Diabetes mellitus-induced lower urinary tract symptoms and hepatic steatosis in an older male
por: Opara, Nnennaya U
Publicado: (2022)

Gastrointestinal manifestations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) patient: major effect on treatment and prognosis
por: Ach, Taieb, et al.
Publicado: (2023)

Recurrent vertebral fractures in a young adult: a closer look at bone health in type 1 diabetes mellitus
por: Thong, Eleanor P, et al.
Publicado: (2018)

Two birds one stone: semaglutide is highly effective against severe psoriasis in a type 2 diabetic patient
por: Costanzo, Gabriele, et al.
Publicado: (2021)

Severe type 2 diabetes (T2D) remission using a very low-calorie ketogenic diet (VLCKD)
por: Correa, Livia Lugarinho, et al.
Publicado: (2022)

Long-lasting response to oral therapy in a young male with monogenic diabetes as part of HNF1B-related disease
por: Carrillo, Elena, et al.
Publicado: (2017)

ACTH-secreting medullary thyroid cancer: a case series
por: Wijewardene, Ayanthi A, et al.
Publicado: (2017)

Thyrotoxic periodic paralysis associated with Graves’ disease: a case series
por: Ludgate, S, et al.
Publicado: (2022)

A clinically novel AIP mutation in a patient with a very large, apparently sporadic somatotrope adenoma
por: Salvatori, Roberto, et al.
Publicado: (2014)

The dilemma of the gender assignment in a Portuguese adolescent with disorder of sex development due to 17β-hydroxysteroid-dehydrogenase type 3 enzyme deficiency
por: Costa, Carla, et al.
Publicado: (2014)

Bilateral adrenal gland haemorrhage: an unusual cause
por: Gowda, Durgesh, et al.
Publicado: (2014)

Pituitary metastases from papillary carcinoma of thyroid: a case report and literature review
por: Chikani, Viral, et al.
Publicado: (2013)

Vanishing hypercalciuric kidney stones after treating underlying acromegaly
por: van der Valk, Eline, et al.
Publicado: (2013)

First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene
por: Casey, R, et al.
Publicado: (2013)

Identification of a novel heterozygous mutation in exon 50 of the COL1A1 gene causing osteogenesis imperfecta
por: Aftab, S A S, et al.
Publicado: (2013)

Radioiodine treatment of differentiated thyroid cancer despite history of ‘iodine allergy’
por: Puchalski, Adam R, et al.
Publicado: (2014)

Tumor-induced osteomalacia due to a recurrent mesenchymal tumor overexpressing several growth factor receptors
por: Yavropoulou, Maria P, et al.
Publicado: (2015)

Pseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene
por: Nobel, Yael R, et al.
Publicado: (2016)

Successful fertility treatment with gonadotrophin therapy for male hypogonadotrophic hypogonadism
por: Rajkanna, J, et al.
Publicado: (2016)

Asymptomatic Paget's disease of bone in a 62-year-old Nigerian man: three years post-alendronate therapy
por: Aransiola, Clement Olukayode, et al.
Publicado: (2016)

Heterogeneity of glucagonomas due to differential processing of proglucagon-derived peptides
por: Challis, Benjamin G, et al.
Publicado: (2015)

Xanthogranulomatous hypophysitis: a rare and often mistaken pituitary lesion
por: Gopal-Kothandapani, Jaya Sujatha, et al.
Publicado: (2015)

Lipoid congenital adrenal hyperplasia due to STAR mutations in a Caucasian patient
por: Kaur, Jasmeet, et al.
Publicado: (2016)

A novel immunopathological association of IgG4-RD and vasculitis with Hashimoto's thyroiditis
por: Minamino, Hiroto, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_o2bvnidgd6vq1jhlh95ma4q6eu