HYPERCALCITONEMIA AND NEONATAL HYPOCALCEMIA
نویسندگان
چکیده
منابع مشابه
Transient neonatal hypocalcemia: presentation and outcomes.
OBJECTIVE To determine the incidence of moderate-to-severe transient neonatal hypocalcemia in term neonates and to describe the characteristics of affected infants and the outcomes of their management. METHODS We reviewed medical records of all term infants <31 days of age who presented to Children's Medical Center Dallas from 2001 to 2009 with hypocalcemia (ionized calcium <1.00 mmol/L [4.00...
متن کاملClinical and laboratory characteristics of neonatal hypocalcemia
PURPOSE To describe the clinical characteristics of full-term neonates with hypocalcemia and to suggest factors associated with neonatal hypocalcemia. METHODS The medical records of full-term neonates with hypocalcemia were reviewed. Hypocalcemia was defined as an ionized calcium (iCa) concentration of <4 mg/dL. Parathyroid hormone (PTH) insufficiency was defined as a serum PTH level of <60 p...
متن کاملPhototherapy Induced Hypocalcemia in Neonatal Hyperbilirubinemia
Background:Jaundice is an important problem in the 1 st week of life affecting approximately 60% of term and 80% of preterm infants. It is commonly managed by phototherapy. Phototherapy may result in the development of hypocalcemia & create serious complications including seizures & other condition. Objective:To study the effect of phototherapy on serum calcium is neonatal hyperbilirubiniea. De...
متن کاملNeonatal hypocalcemia due to asymptomatic maternal primary hyperparathyroidism.
Neonatal hypocalcemia resulting from maternal primary hyperparathyroidism (MPH) is usually detected clinically in the first 2 weeks of life. Occasionally, diagnosis of primary hyperparathyroidism in a young asymptomatic mother is made when the infant presents with hypocalcemia. We present an infant with late onset hypocalcemia resulting from a combination of transient hypoparathyroidism due to ...
متن کاملDiagnostic dilemma: osteopetrosis with superimposed rickets causing neonatal hypocalcemia.
Osteopetrosis is a rare genetic condition of reduced osteoclastic bone resorption which causes defective bone remodeling and skeletal sclerosis during growth, having effects on many organs and tissues. Mutation of T-cell immune regulator 1 (TCRG1) gene is the most common genetic defect leading to osteopetrosis, with poor prognosis. The autosomal recessive form presents in the infantile period (...
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ژورنال
عنوان ژورنال: Pediatric Research
سال: 1977
ISSN: 0031-3998,1530-0447
DOI: 10.1203/00006450-197704000-00332