Compound heterozygous ADAMTS9 variants in Joubert syndrome-related disorders without renal manifestation

• Published in: Brain & development 2022, Vol.44 (2), p.161-165
• Main Authors: Matsushita, Hiroko Baber, Hiraide, Takuya, Hayakawa, Katsumi, Okano, Sozo, Nakashima, Mitsuko, Saitsu, Hirotomo, Kato, Mitsuhiro
• Format: Report
• Language: English
• ISSN: 1872-7131
• DOI: 10.1016/j.braindev.2021.10.004

BACKGROUNDCiliopathies are the outcomes of defects of primary cilia structures and functions which cause multisystemic developmental disorders, such as polycystic kidney disease, nephronophthisis, retinitis pigmentosa, Joubert syndrome (JS), and JS-related disorders (JSRD) with additional organ involvement including oral-facial-digital syndrome and so on. They often share common and unexpected phenotypic features. CASE PRESENTATIONWe report a 4-year-old-boy case with compound heterozygous variants of ADAMTS9. Unlike the cases with ADAMTS9 variants in the previous report, which identified that homozygous variants of ADAMTS9 were responsible for nephronophthisis-related ciliopathies in two cases, the current case did not have nephronophthisis nor renal dysfunction, and his clinical features, such as oculomotor apraxia, hypotonia, developmental delay, bifid tongue, and mild hypoplasia of cerebellar vermis indicated JSRD. CONCLUSIONSThe case suggested a possible association between the clinical presentation of JSRD and ADAMTS9-related disease, and it shows a wide spectrum of ADAMTS9 phenotype.