New-Onset Type 1 Diabetes in a Child with Joubert Syndrome: A Rare Endocrine Complication

<b>Background and Clinical Significance:</b> Joubert syndrome (OMIM #213300) is a rare predominantly autosomal recessive inherited condition characterized by the classic cerebellar vermis hypoplasia and brainstem anomalies (also known as the “molar tooth sign”), hypotonia, and developmen...

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Bibliographic Details
Main Authors: Yutaka Furuta, Erica T. Nelson, Rory J. Tinker, Angela R. Grochowsky
Format: Article
Language:English
Published: MDPI AG 2025-04-01
Series:Reports
Subjects:
Online Access:https://www.mdpi.com/2571-841X/8/2/57
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