Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation. [PDF]
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Heterozygous frameshift KMT2A variant in a patient with Wiedemann-Steiner syndrome. [PDF]
Hum Genome VarHirai S, Mitsubuchi H, Matsumoto S.
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Congenital hypothyroidism with preserved fifth digits in SMARCA4-related Coffin-Siris syndrome: a case report. [PDF]
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Topical Steroid and Fairness Cream Abuse in Facial Dermatoses: A Cross-Sectional Study at a Tertiary Care Center in Western Uttar Pradesh. [PDF]
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Comparative Study on the Therapeutic Efficacy of Topical Bimatoprost (0.03%) Ophthalmic Solution and Tacrolimus (0.1%) Ointment in Stable Vitiligo. [PDF]
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Anterior Cervical Hypertrichosis
Indian Dermatology Online Journal, 2021 Kumar, Piyush, Das, Anupam
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Neuronal Heterotopy in a Patient with Wiedemann-Steiner Syndrome Caused by a Truncating <i>KMT2A</i> Variant: Clinical and Genetic Correlations. [PDF]
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Hyperprolactinemia, hyperandrogenemia, pituitary adenoma, and metabolic disorders in Wiedemann-Steiner syndrome: a case report. [PDF]
BMC Endocr DisordLiang H, Kong J, Li X, Xu X, Zheng C.
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A rare case of H syndrome with severe multisystem involvement: Clinical challenges in low-resource healthcare settings. [PDF]
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