HTLV-1 associated myelopathy/Tropical spastic paraparesis
Jun. 19, 2023
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Characteristic facies with swollen cheeks, narrow sloping forehead, and microcephaly in a 6-year-old child with the PEHO phenotype caused by CCDC88A truncating mutation. (Source: Nahorski MS, Asai M, Wakeling E, et al. CCDC88A mutations cause PEHO-like syndrome in humans and mouse. Brain 2016;139(Pt 4):1036-44. Creative Commons Attribution License.)