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Your search keyword '"Wolcott–Rallison syndrome"' showing total 6 results
Start Over Descriptor "Wolcott–Rallison syndrome" Journal clinical case reports
6 results on '"Wolcott–Rallison syndrome"'

1. The first presentation of Wolcott‐Rallison syndrome in a four‐month‐old infant with diabetic ketoacidosis (DKA) precipitating by COVID‐19: A case report

Author

Elham Maleki, Amir Baniasad, Mina Sepehran, and Najmeh Davoudian

Subjects
coronavirus disease 2019, diabetic ketoacidosis, hyperglycemia, neonatal diabetes, Wolcott‐Rallison syndrome, Medicine, Medicine (General), R5-920
Abstract

Abstract Monogenic diabetes mellitus (eg, Wolcott‐Rallison syndrome) is a rare condition. It associates with neonatal or early‐infancy insulin‐dependent diabetes. We reported DKA in the four‐month infant as the first presentation of monogenic diabetes that has accelerated by COVID‐19 infection. Therefore, considering the concurrency of COVID‐19 and DKA is crucial.

Published
2021
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2. The first presentation of Wolcott‐Rallison syndrome in a four‐month‐old infant with diabetic ketoacidosis (DKA) precipitating by COVID‐19: A case report.

Author

Maleki, Elham, Baniasad, Amir, Sepehran, Mina, and Davoudian, Najmeh

Subjects
COVID-19 pandemic, DIABETIC acidosis, INFANTS, TYPE 1 diabetes, COVID-19
Abstract

Monogenic diabetes mellitus (eg, Wolcott‐Rallison syndrome) is a rare condition. It associates with neonatal or early‐infancy insulin‐dependent diabetes. We reported DKA in the four‐month infant as the first presentation of monogenic diabetes that has accelerated by COVID‐19 infection. Therefore, considering the concurrency of COVID‐19 and DKA is crucial. [ABSTRACT FROM AUTHOR]

Published
2021
Full Text
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3. Practical management in Wolcott‐Rallison syndrome with associated hypothyroidism, neutropenia, and recurrent liver failure: A case report

Author

Markus Lundgren, Elisa De Franco, Henrik Arnell, and Björn Fischler

Subjects
acute liver failure, monogenic diabetes, neonatal diabetes, pediatrics, skeletal dysplasia, Wolcott‐Rallison syndrome, Medicine, Medicine (General), R5-920
Abstract

Key Clinical Message Wolcott‐Rallison syndrome is a rare genetic syndrome of neonatal diabetes, liver failure, and growth retardation. We present a case with a EIF2AK3 p.(Arg902Ter) mutation, additionally complicated by hypothyroidism, impaired renal function, and exocrine pancreas insufficiency, focusing on clinical management. For its optimization, thorough care of multiple organ systems is needed.

Published
2019
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4. Practical management in Wolcott‐Rallison syndrome with associated hypothyroidism, neutropenia, and recurrent liver failure: A case report.

Author

Lundgren, Markus, De Franco, Elisa, Arnell, Henrik, and Fischler, Björn

Subjects
LIVER failure, EXOCRINE pancreatic insufficiency, SYNDROMES, HYPOTHYROIDISM, DWARFISM, NEUTROPENIA
Abstract

Key Clinical Message: Wolcott‐Rallison syndrome is a rare genetic syndrome of neonatal diabetes, liver failure, and growth retardation. We present a case with a EIF2AK3 p.(Arg902Ter) mutation, additionally complicated by hypothyroidism, impaired renal function, and exocrine pancreas insufficiency, focusing on clinical management. For its optimization, thorough care of multiple organ systems is needed. [ABSTRACT FROM AUTHOR]

Published
2019
Full Text
View/download PDF

5. The first presentation of Wolcott‐Rallison syndrome in a four‐month‐old infant with diabetic ketoacidosis (DKA) precipitating by COVID‐19: A case report

Author

Amir Baniasad, Najmeh Davoudian, Elham Maleki, and Mina Sepehran

Subjects
Pediatrics, medicine.medical_specialty, Medicine (General), Diabetic ketoacidosis, Coronavirus disease 2019 (COVID-19), endocrine system diseases, Neonatal diabetes, Case Report, coronavirus disease 2019, diabetic ketoacidosis, R5-920, Diabetes mellitus, medicine, Monogenic Diabetes, Wolcott‐Rallison syndrome, business.industry, nutritional and metabolic diseases, General Medicine, medicine.disease, Medicine, hyperglycemia, Presentation (obstetrics), neonatal diabetes, business, Wolcott–Rallison syndrome
Abstract

Monogenic diabetes mellitus (eg, Wolcott‐Rallison syndrome) is a rare condition. It associates with neonatal or early‐infancy insulin‐dependent diabetes. We reported DKA in the four‐month infant as the first presentation of monogenic diabetes that has accelerated by COVID‐19 infection. Therefore, considering the concurrency of COVID‐19 and DKA is crucial., DKA as an early manifestation of monogenic diabetes (eg, Wolcott‐Rallison syndrome) in infancy, can be accelerated by COVID‐19 infection, so its distinction is imperative in clinical settings.

Published
2021

6. Practical management in Wolcott‐Rallison syndrome with associated hypothyroidism, neutropenia, and recurrent liver failure: A case report

Author

Björn Fischler, Markus Lundgren, Elisa De Franco, and Henrik Arnell

Subjects
Pediatrics, medicine.medical_specialty, Genetic syndromes, pediatrics, Neonatal diabetes, lcsh:Medicine, Case Report, Case Reports, 030204 cardiovascular system & hematology, Neutropenia, skeletal dysplasia, 03 medical and health sciences, 0302 clinical medicine, medicine, EIF2AK3, Organ system, Wolcott‐Rallison syndrome, lcsh:R5-920, business.industry, lcsh:R, Liver failure, General Medicine, acute liver failure, medicine.disease, 3. Good health, 030220 oncology & carcinogenesis, monogenic diabetes, neonatal diabetes, lcsh:Medicine (General), business, Wolcott–Rallison syndrome, Exocrine Pancreas Insufficiency
Abstract

Key Clinical Message Wolcott‐Rallison syndrome is a rare genetic syndrome of neonatal diabetes, liver failure, and growth retardation. We present a case with a EIF2AK3 p.(Arg902Ter) mutation, additionally complicated by hypothyroidism, impaired renal function, and exocrine pancreas insufficiency, focusing on clinical management. For its optimization, thorough care of multiple organ systems is needed.

Published
2019

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