Searchable abstracts of presentations at key conferences in endocrinology

ea0022p797 | Thyroid | ECE2010

Reversible thyrotoxic cardiomyopathy

Nasser Tariq , Kjnsarah Abdulhalim , Karawgh Abdullah

A 47-year-old, previously healthy, ex-smoker male presented with a two-week history of dyspnea grade 4 with progressive course, palpitations, orthopnea, and paroxysmal nocturnal dyspnea. There was no history of chest pain or fever, but he had noticed recent an unintentional 10 to 15 kg weight loss over the previous 3 months. There was no previous history of cardiorespiratory problems, hypertension, and diabetes. On examination he was dyspenic, anxious and tremulous. His temper...

ea0022p380 | Endocrine tumours &amp; neoplasia (<emphasis role="italic">Generously supported by Novartis</emphasis>) | ECE2010

RET codon 618 mutations is the most frequent phenotype in Saudi families with multiple endocrine neoplasia type 2A

Nasser Tariq , Qari Faiza , Karawgh Abdullah , Al Aama Jumanah

Objective: To evaluate the prevalence of the RET mutation and the genotype–phenotype relation in Saudi patients (families) with multiple endocrine neoplasia type 2A (MEN2A) or familial medullary thyroid carcinoma (FMTC).Design: Cross-sectional study.Patients and methods: A total of ten unrelated Saudi families with germline mutation of the RET protooncogene and/or immunohistochemistry diagnosis of MTC were identified. B...