Sporadic association of Legg–Calve–Perthes disease with rare phakomatoses-Gomez-Lopez-Hernandez syndrome

Balaji Zacharia, Thanveeruddin Sherule, Dhiyaneswaran Subramaniam, R. Purushothaman
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Abstract

Gomez-Lopez-Hernandez syndrome (GLH) is a very rare phakomatosis, which is characterized by the triad of rhombencephalosynapsis, facial anesthesia in the trigeminal area, and scalp alopecia. A 9-year-old boy with pain and limping right hip for 6 months was presented. Clinically, he was having bilateral symmetrical temporal alopecia, strabismus, and pseudoproptosis. Magnetic resonance imaging brain shows cerebellar fusion. Examination of the hip was consistent with the diagnosis of Perthes disease. Even though some of the phakomatoses are associated with skeletal abnormalities, there is no association of any phakomatoses with Legg–Calve–Perthes disease (LCPD) of the hip. This will be the first ever report of an association of GLH syndrome with LCPD.
legg - calf - perthes病与罕见的肉瘤- gomez - lopez - hernandez综合征的散发关联
Gomez-Lopez-Hernandez综合征(GLH)是一种非常罕见的斑疹性疾病,其特征是菱形脑突触、三叉神经区面部麻醉和头皮脱发。我们介绍了一名9岁男孩,右髋关节疼痛和跛行6个月。临床表现为双侧对称性颞部脱发、斜视、假眼突出。脑磁共振成像显示小脑融合。髋关节检查与Perthes病的诊断一致。尽管一些吞噬病与骨骼异常有关,但没有任何吞噬病与髋关节的legg - calf - perthes病(LCPD)有关。这将是首次报道GLH综合征与LCPD的关联。
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