An Early Rare MEN1 Phenotype Abstract #968

Introduction: A 13-yr-old boy was referred to our department for short stature.
Aim(s):
Materials and methods: His family history was relevant for MEN1 syndrome and he was known to have MEN1 germline mutation from the age of 6. He reported occasional headaches. Physical examination revealed overweight (75th percentile), short stature (3rd percentile) and face rubeosis.
Conference: 11th Annual ENETS Conference 2014 (2014)
Category: Clinical cases/reports
Presenting Author: Marialberta Battocchio
Keywords: MEN1, hypercorticism

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