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Alström syndrome: A novel mutation in Saudi girl with insulin-resistant diabetes

RATIONALE: Alström syndrome is an autosomal recessive disorder characterized by hearing loss, blindness, obesity, non-insulin dependent diabetes, and others. PATIENT CONCERN: A 10 years old Saudi girl, who presented with diabetic ketoacidosis and found to have hearing loss and blindness. DIAGNOSIS:...

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Autores principales: Bakar, Ayman A., Kamal, Naglaa Mohamed, Alsaedi, Abdulaziz, Turkistani, Reem, Aldosari, Dima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348158/
https://www.ncbi.nlm.nih.gov/pubmed/28272210
http://dx.doi.org/10.1097/MD.0000000000006192
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author Bakar, Ayman A.
Kamal, Naglaa Mohamed
Alsaedi, Abdulaziz
Turkistani, Reem
Aldosari, Dima
author_facet Bakar, Ayman A.
Kamal, Naglaa Mohamed
Alsaedi, Abdulaziz
Turkistani, Reem
Aldosari, Dima
author_sort Bakar, Ayman A.
collection PubMed
description RATIONALE: Alström syndrome is an autosomal recessive disorder characterized by hearing loss, blindness, obesity, non-insulin dependent diabetes, and others. PATIENT CONCERN: A 10 years old Saudi girl, who presented with diabetic ketoacidosis and found to have hearing loss and blindness. DIAGNOSIS: Alström syndrome. INTERVENTIONS: Multidisciplinary team approach, with echocardiography, hearing test, eye exam and genetic test for Alström syndrome. OUTCOMES: The patient has retinitis pigmentosa, bilateral hearing loss, double diabetes with weakly positive anti-insulin antibodies and DNA analysis showed novel mutation for Alström syndrome. LESSONS: the combination of obesity, diabetes, hearing loss and blindness should alert the physician to test for Alström syndrome.
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spelling pubmed-53481582017-03-22 Alström syndrome: A novel mutation in Saudi girl with insulin-resistant diabetes Bakar, Ayman A. Kamal, Naglaa Mohamed Alsaedi, Abdulaziz Turkistani, Reem Aldosari, Dima Medicine (Baltimore) 6200 RATIONALE: Alström syndrome is an autosomal recessive disorder characterized by hearing loss, blindness, obesity, non-insulin dependent diabetes, and others. PATIENT CONCERN: A 10 years old Saudi girl, who presented with diabetic ketoacidosis and found to have hearing loss and blindness. DIAGNOSIS: Alström syndrome. INTERVENTIONS: Multidisciplinary team approach, with echocardiography, hearing test, eye exam and genetic test for Alström syndrome. OUTCOMES: The patient has retinitis pigmentosa, bilateral hearing loss, double diabetes with weakly positive anti-insulin antibodies and DNA analysis showed novel mutation for Alström syndrome. LESSONS: the combination of obesity, diabetes, hearing loss and blindness should alert the physician to test for Alström syndrome. Wolters Kluwer Health 2017-03-10 /pmc/articles/PMC5348158/ /pubmed/28272210 http://dx.doi.org/10.1097/MD.0000000000006192 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0
spellingShingle 6200
Bakar, Ayman A.
Kamal, Naglaa Mohamed
Alsaedi, Abdulaziz
Turkistani, Reem
Aldosari, Dima
Alström syndrome: A novel mutation in Saudi girl with insulin-resistant diabetes
title Alström syndrome: A novel mutation in Saudi girl with insulin-resistant diabetes
title_full Alström syndrome: A novel mutation in Saudi girl with insulin-resistant diabetes
title_fullStr Alström syndrome: A novel mutation in Saudi girl with insulin-resistant diabetes
title_full_unstemmed Alström syndrome: A novel mutation in Saudi girl with insulin-resistant diabetes
title_short Alström syndrome: A novel mutation in Saudi girl with insulin-resistant diabetes
title_sort alström syndrome: a novel mutation in saudi girl with insulin-resistant diabetes
topic 6200
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348158/
https://www.ncbi.nlm.nih.gov/pubmed/28272210
http://dx.doi.org/10.1097/MD.0000000000006192
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