Zobrazeno 1 - 10
of 63
pro vyhledávání: '"MODY 5"'
Autor:
Sixu Xin, Xiaomei Zhang
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundMaturity-onset diabetes of the young type 5 (MODY5) is an uncommon, underrecognized condition that can be encountered in several clinical contexts. It is challenging to diagnose because it is considered rare and therefore overlooked in the
Externí odkaz:
https://doaj.org/article/15e5b1c325d24ddb82ea6f8c6bb37a6b
Akademický článek
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Autor:
Patouni, Konstantina a, ∗, Cinek, Ondrej b, Pruhova, Stepanka b, Elblova, Lenka b, Xatzipsalti, Maria a, Sertedaki, Amalia c, Vazeou, Andriani a
Publikováno v:
In European Journal of Medical Genetics September 2021 64(9)
Autor:
Khushboo Agarwal, MBBS, MD, Aaron Chapla, MSC, PhD, Anuradha Chandramohan, MBBS, MD, Chandra J. Singh, MS, MCh, DNB, Nihal Thomas, MBBS, MD, DNB, PhD, Felix K. Jebasingh, MBBS, MD, DM, DNB
Publikováno v:
AACE Clinical Case Reports, Vol 8, Iss 1, Pp 22-24 (2022)
Objective: Maturity-onset diabetes of the young (MODY) type 5 is caused by an autosomal dominant mutation in the HNF1B gene. Our objective was to report a case of a young girl with bicornuate uterus and recurrent renal stones with diabetes mellitus (
Externí odkaz:
https://doaj.org/article/75bffca71c1d49e2829877127a2fdfc7
Publikováno v:
BMC Endocrine Disorders, Vol 18, Iss 1, Pp 1-8 (2018)
Abstract Background The diagnosis of atypical non-autoimmune forms of diabetes mellitus, such as maturity onset diabetes of the young (MODY) presents several challenges, in view of the extensive clinical and genetic heterogeneity of the disease. In t
Externí odkaz:
https://doaj.org/article/e9532d32463546308a344c0895c163fa
Autor:
Joon Kim, Nicholas Ng, Marie Burke, Najia Siddique, Matilde Bettina Mijares Zamuner, Maria M. Byrne
Publikováno v:
Acta Diabetologica. 59:83-93
Molecular defects of hepatic nuclear factor 1β (HNF1β) are associated with multiorgan disease (renal disease, pancreatic hypoplasia, and genital tract anomalies) in addition to diabetes. We examined the phenotypic features, insulin secretory respon
Autor:
Aaron Chapla, Khushboo Agarwal, Anuradha Chandramohan, Felix K Jebasingh, Chandra Singh, Nihal Thomas
Publikováno v:
AACE Clinical Case Reports, Vol 8, Iss 1, Pp 22-24 (2022)
AACE Clinical Case Reports
AACE Clinical Case Reports
Objective Maturity-onset diabetes of the young (MODY) type 5 is caused by an autosomal dominant mutation in the HNF1B gene. Our objective was to report a case of a young girl with bicornuate uterus and recurrent renal stones with diabetes mellitus (D
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-8 (2021)
BMC Pediatrics
BMC Pediatrics
Background The prevalence of monogenic diabetes is estimated to be 1.1–6.3% of patients with diabetes mellitus (DM) in Europe. The overlapping clinical features of various forms of diabetes make differential diagnosis challenging. Therefore, this s
Autor:
Ren Jie Jacob Chew, Hoe Kit Chee
Publikováno v:
Clinical Advances in Periodontics. 11:64-69
Introduction Maturity onset diabetes of the young (MODY) is a rare form of diabetes mellitus resulting from single nucleotide polymorphisms. There is a lack of evidence describing their periodontal condition and the management of these patients. The
Akademický článek
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