Description of the first genetically confirming case with Donahue’s syndrome in Russia
https://doi.org/10.14341/probl201662242-45
Abstract
Syndrome Donahue (leprechaunism) is a rare form of neonatal diabetes mellitus associated with INSR gene mutations.
There are three types of insulin resistance syndrome: Donohue syndrome, Rabson—Mendenhall syndrome and insulin resistance type A. These syndromes are distinguished from one another by severity of symptoms, age of onset and age of death. Donohue and Rabson—Mendenhall syndromes are associated with biallelic mutations in the α-subunit or/and β-subunit of INSR gene and are characterized by more severe phenotype and poor prognosis. Patients with Donohue syndrome usually die within the first two years of life. Life expectancy of patients with Rabson—Mendenhall syndrome is 5—15 years.
Most patients with insulin resistance type A have heterozygous mutations in the β-subunit and demonstrate mild phenotype.
Here, we describe the first genetically confirmed case of syndrome Donahue in the Russian Federation.
Keywords
About the Authors
Yulia V. TikhonovichRussian Federation
MD, PhD, Assistant researcher
Competing Interests: конфликт интересов отсутствует
Oleg A. Malievsky
Russian Federation
MD, PhD, Professor
Competing Interests: конфликт интересов отсутствует
Anatoly Tyul'pakov
Russian Federation
MD, PhD, Head of the Generic endocrinopathies department, Clinical Endocrinology Institute
Competing Interests: конфликт интересов отсутствует
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Supplementary files
Review
For citations:
Tikhonovich Yu.V., Malievsky O.A., Tyul'pakov A. Description of the first genetically confirming case with Donahue’s syndrome in Russia. Problems of Endocrinology. 2016;62(2):42-45. https://doi.org/10.14341/probl201662242-45

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