A case report of McCune–Albright syndrome with hepatic manifestations

McCune–Albright syndrome is a non‐hereditary disease characterized by café‐au‐lait skin spots, fibrous dysplasia of bone, and endocrinopathies. We report a boy with a history of repeated hospitalizations from birth due to severe jaundice and hyperthyroidism. At the age of 2 years, he suffered from a...

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Autores principales: Haddadi, Mohammad, Lal Kheirkhah, Elahe, Ansari, Mojgan, Ahmadzade, Samieh, Taraz, Zeinab, Yazdi, Saeid
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/PMC9295684/
https://www.ncbi.nlm.nih.gov/pubmed/35865771
http://dx.doi.org/10.1002/ccr3.6077
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author Haddadi, Mohammad
Lal Kheirkhah, Elahe
Ansari, Mojgan
Ahmadzade, Samieh
Taraz, Zeinab
Yazdi, Saeid
author_facet Haddadi, Mohammad
Lal Kheirkhah, Elahe
Ansari, Mojgan
Ahmadzade, Samieh
Taraz, Zeinab
Yazdi, Saeid
author_sort Haddadi, Mohammad
collection PubMed
description McCune–Albright syndrome is a non‐hereditary disease characterized by café‐au‐lait skin spots, fibrous dysplasia of bone, and endocrinopathies. We report a boy with a history of repeated hospitalizations from birth due to severe jaundice and hyperthyroidism. At the age of 2 years, he suffered from a proximal left femoral fracture. During the follow‐up, liver function tests were abnormal. Considering the clinical and paraclinical findings, the patient was diagnosed with McCune–Albright syndrome.
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spelling pubmed-92956842022-07-20 A case report of McCune–Albright syndrome with hepatic manifestations Haddadi, Mohammad Lal Kheirkhah, Elahe Ansari, Mojgan Ahmadzade, Samieh Taraz, Zeinab Yazdi, Saeid Clin Case Rep Case Report McCune–Albright syndrome is a non‐hereditary disease characterized by café‐au‐lait skin spots, fibrous dysplasia of bone, and endocrinopathies. We report a boy with a history of repeated hospitalizations from birth due to severe jaundice and hyperthyroidism. At the age of 2 years, he suffered from a proximal left femoral fracture. During the follow‐up, liver function tests were abnormal. Considering the clinical and paraclinical findings, the patient was diagnosed with McCune–Albright syndrome. John Wiley and Sons Inc. 2022-07-19 /pmc/articles/PMC9295684/ /pubmed/35865771 http://dx.doi.org/10.1002/ccr3.6077 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Report
Haddadi, Mohammad
Lal Kheirkhah, Elahe
Ansari, Mojgan
Ahmadzade, Samieh
Taraz, Zeinab
Yazdi, Saeid
A case report of McCune–Albright syndrome with hepatic manifestations
title A case report of McCune–Albright syndrome with hepatic manifestations
title_full A case report of McCune–Albright syndrome with hepatic manifestations
title_fullStr A case report of McCune–Albright syndrome with hepatic manifestations
title_full_unstemmed A case report of McCune–Albright syndrome with hepatic manifestations
title_short A case report of McCune–Albright syndrome with hepatic manifestations
title_sort case report of mccune–albright syndrome with hepatic manifestations
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9295684/
https://www.ncbi.nlm.nih.gov/pubmed/35865771
http://dx.doi.org/10.1002/ccr3.6077
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