A case report of H‐syndrome from Baghdad Medical City treated with tocilizumab

This case report presents the first H‐syndrome rarity in Iraq, a 12‐year‐old female patient who was attending the Rheumatology out clinic for progressive hands joint deformities. She has a history of a multi‐systemic collection of diseases with various clinical features that include beta thalassemia...

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Autores principales: Awadh, Nabaa Ihsan, Gorial, Faiq I., Hashim, Hashim Talib, Al‐Obaidi, Ahmed Dheyaa, Al‐Obaidi, Mustafa Najah, AlNoori, Ali H., Aljanabi, Wesal K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9761660/
https://www.ncbi.nlm.nih.gov/pubmed/36545557
http://dx.doi.org/10.1002/ccr3.6775
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author Awadh, Nabaa Ihsan
Gorial, Faiq I.
Hashim, Hashim Talib
Al‐Obaidi, Ahmed Dheyaa
Al‐Obaidi, Mustafa Najah
AlNoori, Ali H.
Aljanabi, Wesal K.
author_facet Awadh, Nabaa Ihsan
Gorial, Faiq I.
Hashim, Hashim Talib
Al‐Obaidi, Ahmed Dheyaa
Al‐Obaidi, Mustafa Najah
AlNoori, Ali H.
Aljanabi, Wesal K.
author_sort Awadh, Nabaa Ihsan
collection PubMed
description This case report presents the first H‐syndrome rarity in Iraq, a 12‐year‐old female patient who was attending the Rheumatology out clinic for progressive hands joint deformities. She has a history of a multi‐systemic collection of diseases with various clinical features that include beta thalassemia minor, sensorineural deafness, and celiac disease.
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spelling pubmed-97616602022-12-20 A case report of H‐syndrome from Baghdad Medical City treated with tocilizumab Awadh, Nabaa Ihsan Gorial, Faiq I. Hashim, Hashim Talib Al‐Obaidi, Ahmed Dheyaa Al‐Obaidi, Mustafa Najah AlNoori, Ali H. Aljanabi, Wesal K. Clin Case Rep Case Report This case report presents the first H‐syndrome rarity in Iraq, a 12‐year‐old female patient who was attending the Rheumatology out clinic for progressive hands joint deformities. She has a history of a multi‐systemic collection of diseases with various clinical features that include beta thalassemia minor, sensorineural deafness, and celiac disease. John Wiley and Sons Inc. 2022-12-19 /pmc/articles/PMC9761660/ /pubmed/36545557 http://dx.doi.org/10.1002/ccr3.6775 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Awadh, Nabaa Ihsan
Gorial, Faiq I.
Hashim, Hashim Talib
Al‐Obaidi, Ahmed Dheyaa
Al‐Obaidi, Mustafa Najah
AlNoori, Ali H.
Aljanabi, Wesal K.
A case report of H‐syndrome from Baghdad Medical City treated with tocilizumab
title A case report of H‐syndrome from Baghdad Medical City treated with tocilizumab
title_full A case report of H‐syndrome from Baghdad Medical City treated with tocilizumab
title_fullStr A case report of H‐syndrome from Baghdad Medical City treated with tocilizumab
title_full_unstemmed A case report of H‐syndrome from Baghdad Medical City treated with tocilizumab
title_short A case report of H‐syndrome from Baghdad Medical City treated with tocilizumab
title_sort case report of h‐syndrome from baghdad medical city treated with tocilizumab
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9761660/
https://www.ncbi.nlm.nih.gov/pubmed/36545557
http://dx.doi.org/10.1002/ccr3.6775
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