ABSTRACT Smith‐Magenis Syndrome (SMS) is an uncommon genetic disorder caused by microdeletions of chromosome 17p11.2 including the RAI1 gene, or loss‐of‐function mutations that directly affect RAI1. Due to the involvement of RAI1 in neurodevelopment, SMS leads to typical pathologic features in the behavioral and physical phenotype that must be ...
Edgar Andrés Chavarría‐Martínez +4 more
wiley +1 more source
Management of Thyroid Eye Disease: A Comparison Between Three Recent Clinical Guidelines. [PDF]
Lei C +7 more
europepmc +1 more source
Solid Subtype of Papillary Thyroid Carcinoma: A Case Series Highlighting Aggressive Features
Hematoxylin and eosin (H&E) stained section, 40×. Tumor cells with “Orphan Annie eye” nuclei arranged in solid nests. ABSTRACT Papillary thyroid carcinoma (PTC) is the most common malignant thyroid neoplasm. Its solid/trabecular subtype (STPTC) is rare, and its aggressiveness remains controversial.
Rafael Castellanos Bueno +4 more
wiley +1 more source
Retinal Microvascular and Orbital Structural Alterations in Thyroid Eye Disease. [PDF]
Jelušić V +8 more
europepmc +1 more source
When Antibiotics Leave a Mark: Minocycline‐Induced Hyperpigmentation
Bluish discoloration of the dorsal aspects of the hands and nails. ABSTRACT This article presents two patients with significant minocycline‐induced hyperpigmentation, illustrating the diverse clinical manifestations across various body sites. Judicious use of minocycline and early recognition of its adverse effects are crucial to reduce the risk of ...
Clarissa Ting +3 more
wiley +1 more source
Is there a role of radiotherapy for steroid-resistant thyroid eye disease? [PDF]
Noh JM.
europepmc +1 more source
Familial Mediterranean fever in northwest of Iran (Ardabil): The first global report from Iran [PDF]
Familial Mediterranean fever (FMF), which is the prototype of the hereditary periodic fever syndromes, is common in the countries around the Mediterranean Sea. Considering its geographical position in the northwest of Iran, with its population of Turkish
امامی, دینا +10 more
core
Severe Headache and Acute Blindness: A Case of Pituitary Apoplexy
ABSTRACT Pituitary apoplexy is a rare, life‐threatening syndrome that commonly occurs in the adenomatous pituitary gland. It presents with a myriad of severe neuroendocrine and ophthalmological signs and symptoms. Early diagnosis and prompt treatment are vital in the management of pituitary apoplexy.
Abdul‐Rahman Faiza +4 more
wiley +1 more source
Quantification of enlargement of the levator palpebrae superioris muscle in thyroid eye disease. [PDF]
Hains L +4 more
europepmc +1 more source
Cell migration, chimerism, and graft acceptance [PDF]
A.J Demetris +47 more
core +1 more source

