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Journal of Korean Medical Science ; : 1682-1686, 2013.
Article in English | WPRIM | ID: wpr-148456

ABSTRACT

A 21-year-old man with diabetic ketoacidosis (DKA) displayed short and clubbed fingers and marked eyebrow, which are typical of Hajdu-Cheney Syndrome (HCS). Laboratory findings confirmed type 1 diabetes mellitus (DM). After conservative care with hydration and insulin supply, metabolic impairment was improved. Examinations of bone and metabolism revealed osteoporosis and craniofacial abnormalities. The mutation (c.6443T>G) of the NOTCH2 gene was found. The patient was diagnosed with HCS and DM. There may be a relationship between HCS and DM, with development of pancreatic symptoms related to the NOTCH2 gene mutation.


Subject(s)
Adult , Humans , Male , Young Adult , Bone Density , Craniofacial Abnormalities/complications , Diabetes Mellitus, Type 1/complications , Diabetic Ketoacidosis/complications , Glycosuria , Hajdu-Cheney Syndrome/complications , Ketone Bodies/urine , Mutation , Osteoporosis/complications , Receptor, Notch2/genetics
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