Graves′ disease with thyroid hemiagenesis: A rare abnormality with rarer presentation

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Thyroid hemiagenesis with Graves' disease, Graves' ophthalmopathy and multinodular goiter.

Thyroid hemiagenesis is a rare congenital anomaly in which one of the thyroid lobes with or without isthmus fails to develop. Here we present a woman patient with thyroid hemiagenesis, Graves' disease and ophthalmopathy with nodular goiter. Fine needle aspiration biopsy of the dominant nodule was suspicious of malignancy. The patient was referred for surgery for total thyroidectomy. Histopathol...

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rare association of schizophrenia and unilateral graves’ disease with contralateral thyroid hemiagenesis in two cases of mccune-albright syndrome

the classical triad of mccune-albright syndrome (mas) consists of polyostotic fibrous dysplasia (fd), skin hyperpigmentation (café-au-lait spots), and endocrine dysfunction, frequently seen in females as precocious puberty. etiology is genetically based and is explained by mosaicism of activating somatic mutations of the alpha-subunit of gs protein. clinical presentation is varied and is depend...

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ژورنال

عنوان ژورنال: Indian Journal of Nuclear Medicine

سال: 2014

ISSN: 0972-3919

DOI: 10.4103/0972-3919.130321