Purpose: KBG syndrome (KBGS) is a rare neurodevelopmental syndrome caused by haploinsufficiency of ANKRD11. The childhood phenotype is extensively reported but limited for adults. Thus, we aimed to delineate the clinical features of KBGS. Methods: We collected physician-reported data of adults with molecularly confirmed KBGS through an international collaboration. Moreover, we undertook a systematic literature review to determine the scope of previously reported data. Results: The international collaboration identified 36 adults from 31 unrelated families with KBGS. Symptopms included mild/borderline intellectual disability (n=22); gross and/or fine motor difficulties (n=15); psychiatric and behavioral comorbidities including aggression, anxiety, reduced attention span, and autistic features (n=26); nonverbal (n=3), seizures with various seizure types and treatment responses (n=10); ophthalmological comorbidities (n=20). Cognitive regression during adulthood was reported once. Infrequent features included dilatation of the ascending aorta (n=2) and autoimmune conditions (n=4). Education, work, and residence varied and the diversity of professional and personal roles highlighted the range of abilities seen. The literature review identified 154 adults reported across the literature, and we have summarized the features across both datasets. Conclusion: Our study sheds light on the long-term neurodevelopmental outcomes, seizures, behavioral and psychiatric features, and education, work, and living arrangements for adults with KBGS.

Natural history of adults with KBG syndrome: a physician-reported experience / A. Bayat, H. Grimes, E. de Boer, M.K. Herlin, R.S. Dahl, I.C.B. Lund, M. Bayat, A.C. Skjelmose Bolund, C.E. Gjerulfsen, P.A. Gregersen, M. Zilmer, S. Juhl, K. Cebula, E. Rahikkala, I. Maystadt, A. Peron, A. Vignoli, R.M. Alfano, F. Stanzial, F. Benedicenti, A. Currò, H. Luk, G. Jouret, E. Zurita, L. Heuft, F. Schnabel, A. Busche, H.E. Veenstra-Knol, T. Tkemaladze, P. Vrielynck, D. Lederer, K. Platzer, C.W. Ockeloen, H. Goel, K.J. Low. - In: GENETICS IN MEDICINE. - ISSN 1098-3600. - 26:8(2024 Aug), pp. 101170.1-101170.13. [Epub ahead of print] [10.1016/j.gim.2024.101170]

Natural history of adults with KBG syndrome: a physician-reported experience

A. Peron;A. Vignoli;
2024

Abstract

Purpose: KBG syndrome (KBGS) is a rare neurodevelopmental syndrome caused by haploinsufficiency of ANKRD11. The childhood phenotype is extensively reported but limited for adults. Thus, we aimed to delineate the clinical features of KBGS. Methods: We collected physician-reported data of adults with molecularly confirmed KBGS through an international collaboration. Moreover, we undertook a systematic literature review to determine the scope of previously reported data. Results: The international collaboration identified 36 adults from 31 unrelated families with KBGS. Symptopms included mild/borderline intellectual disability (n=22); gross and/or fine motor difficulties (n=15); psychiatric and behavioral comorbidities including aggression, anxiety, reduced attention span, and autistic features (n=26); nonverbal (n=3), seizures with various seizure types and treatment responses (n=10); ophthalmological comorbidities (n=20). Cognitive regression during adulthood was reported once. Infrequent features included dilatation of the ascending aorta (n=2) and autoimmune conditions (n=4). Education, work, and residence varied and the diversity of professional and personal roles highlighted the range of abilities seen. The literature review identified 154 adults reported across the literature, and we have summarized the features across both datasets. Conclusion: Our study sheds light on the long-term neurodevelopmental outcomes, seizures, behavioral and psychiatric features, and education, work, and living arrangements for adults with KBGS.
ANKRD11; KBGS; adult; neurodevelopment; seizure
Settore MED/39 - Neuropsichiatria Infantile
Settore MED/03 - Genetica Medica
ago-2024
27-mag-2024
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1062208
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