Menü Kapat

A girl diagnosed with familial hypocalciuric hypercalcemia with heterozygous p.Cys575Tyr variation in the CaSR gene

Case Report

A girl diagnosed with familial hypocalciuric hypercalcemia with heterozygous p.Cys575Tyr variation in the CaSR gene

Receiving Date: 22 August 2022

Accept Date: 06 November 2022

Available Online: 28 November 2022

doi: 10.5455/medscience.2022.08.193
Med-Science. 2022;11(4):1731-3

Conflict of interests
The authors declare that there is no conflict of interest in the study.

Financial Disclosure
The authors declare that they have received no financial support for the study.

Informed consent
Informed consent forms were obtained from the parents of the patients for publication of the cases, including images.

 222 total views,  137 views today

CITATION
Dundar I. Camtosun E. Dogan M. et al. A girl diagnosed with familial hypocalciuric hypercalcemia with heterozygous p.Cys575Tyr variation in the CaSR gene. Medicine Sci. 2022;11(4):1731-3

⇓ PlumX Meter

Corresponding Author: Ismail Dundar, Inonu University, Faculty of Medicine, Department of Pediatric Endocrinology, Malatya, Türkiye
E-mail: ismail.dundar@inonu.edu.tr

Evaluation of endocrine functions before and after enzyme replacement therapy in children with mucopolysaccharidosis

Orjinal Article

Evaluation of endocrine functions before and after enzyme replacement therapy in children with mucopolysaccharidosis

Receiving Date: 04 March 2022

Accept Date:15 June 2022

Available Online: 08.08.2022

doi: 10.5455/medscience.2022.03.053

Medicine Science 2022;11(3):1184-9

Conflict of interests: The authors declare that there is no conflict of interest in the study.
Financial Disclosure: The authors declare that they have received no financial support for the study.
Ethical approval: Subjects were enrolled following approval of the study protocol by the medical ethics committee (Ethics Committee of the Inonu University, approval number: 2021/2064), and receipt of written informed consent from parents.

 1,808 total views,  9 views today

Dundar I, Cifci N, Akinci A, et al.
Evaluation of endocrine functions before and after enzyme replacement therapy in children with mucopolysaccharidosis . Med Science. 2022;11(3):1184-9.

⇓ PlumX Meter

Corresponding Author: Kutay Saglam, Inonu University, Faculty of Medical, Department of Gastrointestinal Surgery, Liver Transplantation Institute, Malatya, Turkey.
E-mail: saglamk@gmail.com

The relationship between autoimmunity and HbA1c in type 1 diabetes mellitus patients

Original Article

The relationship between autoimmunity and HbA1c in type 1 diabetes mellitus patients

Dilvin Celik Ates, Aysehan Akinci, Ismail Dundar

Abstract

Indicators of increased risk for type 1 diabetes (T1DM) are specific antibodies that are mainly immune markers. Islet cell antibody (ICA), insulin autoantibody (IAA), glutamic acid decarboxylase enzyme antibody (GADA) and HgA1c are also used in the diagnosis and follow-up of patients with type 1 diabetes mellitus. ICA, IAA, GADA, HbA1c were checked at the time of diagnosis and at 6-month intervals in pediatric patients monitored with T1DM. Decreased ICA, GADA and HbA1c levels were evaluated as good blood glucose control and good clinical response. Patients aged ≤5 years had a higher rate of IAA and patients aged >5 years had a higher rate of ICA. Antibody selection according to age during diabetes screening was found to be significant in terms of cost.

Key words: Diabetes mellitus, autoantibody, glycolyzed hemoglobin

Med-Science. 2021; 10(4): 1505-9