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A Case of Joubert Syndrome with Chronic Kidney Disease

Joubert syndrome is a genetically heterogeneous disorder that belongs to the group of cerebello-oculo-renal syndromes. It is characterised by neurodevelopmental abnormalities and complex midbrain-hindbrain malformation, visible on brain imaging as a molar tooth sign. It is classified as a ciliopathy...

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Detalles Bibliográficos
Autores principales: Shamsudheen, M. P., Das, Uttara, Taduri, Gangadhar, Guditi, Swarnalatha, Karthik, Raja, Thakur, Rajani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8101675/
https://www.ncbi.nlm.nih.gov/pubmed/33994691
http://dx.doi.org/10.4103/ijn.IJN_287_19
Descripción
Sumario:Joubert syndrome is a genetically heterogeneous disorder that belongs to the group of cerebello-oculo-renal syndromes. It is characterised by neurodevelopmental abnormalities and complex midbrain-hindbrain malformation, visible on brain imaging as a molar tooth sign. It is classified as a ciliopathy and has variable renal involvement. Herein, we report a case of a 9-year-old boy with developmental delay, presented as chronic kidney disease and evaluation showed features of Joubert syndrome. Recognition of specific clinical and radiological findings will help in early diagnosis and appropriate care.