Publications by authors named "Rotem Agur"
Background: Hypoparathyroidism, retardation, and dysmorphism (HRD) Syndrome is a rare disease composed of hypoparathyroidism, retardation of both growth and development, and distinctive dysmorphic features. Here, we describe the long-term morbidity and mortality in a large cohort of HRD patients and suggest recommendations for follow up and treatment.
Methods: Medical records of 63 HRD syndrome patients who were followed at Soroka Medical Center during 1989-2019 were reviewed retrospectively.
Multiple Endocrine Deficiencies are Common in Hypoparathyroidism-Retardation-Dysmorphism Syndrome.
J Clin Endocrinol Metab
January 2021
Article Synopsis
- * A study of 63 HRD patients showed all were born small for gestational age and had severe growth retardation, with significant rates of hypoglycemia and growth hormone deficiency.
- * The findings also revealed various hormonal deficiencies, prompting recommendations for regular screening of thyroid and adrenal functions in these patients.