Searchable abstracts of presentations at key conferences on calcified tissues

ba0001pp123 | Calciotropic and phosphotropic hormones and mineral metabolism | ECTS2013

Vitamin D supplementation during lactation: effect on maternal and offspring's vitamin D status and bone mass–double-blind randomized control trial

Czech-Kowalska Justyna , Jaworski Maciej , Latka-Grot Julita , Bulsiewicz Dorota , Pludowski Pawel , Chazan Bogdan , Pawlus Beata , Wygledowska Grazyna , Zochowska Anna , Kornacka Maria K , Kryskiewicz Edyta , Karczmarewicz Elzbieta , Dobrzanska Anna

Introduction: Optimal vitamin D intake for lactating women remains controversial. We hypothesized that 1200 IU/day (vs 400 IU/day) of vitamin D during breastfeeding will enhance maternal vitamin D status and bone mass.Methods: Healthy mothers after term, singleton delivery were randomized to receive vitamin D3: 1200 IU/day (800+400 IU/day from multivitamins) or 400 IU/day (placebo+400 IU/day from multivitamins) during lactation. Serum 25-hydroxyvitamin D...

ba0003pp377 | Other diseases of bone and mineral metabolism | ECTS2014

Fine-needle aspiration with PTH measurement facilitates minimally invasive parathyroidectomy – report of two cases

Grigorie Daniel , Ioachim Dumitru , Stanescu Bogdan , Sucaliuc Alina , Caragheorgheopol Andra

Objective: Minimally invasive parathyroidectomy (MIP) has become a frequently used strategy but it requires a precise preoperative localization and the use of intraoperative PTH to fulfill its benefits. The current localization techniques (ultrasonography, MIBI scan) have shortcomings and intraoperative PTH is not available in our country.Case presentation: We report the cases of two patients, females (63 and 55 years old), with clinical and biochemical ...

ba0006p071 | (1) | ICCBH2017

In search of hypophosphatasia: a need to establish normative data for low alkaline phosphatase in pediatric population

Abramowicz Pawel , Konstantynowicz Jerzy , Zelazowska-Rutkowska Beata , Cylwik Bogdan

Background: Hypophosphatasia (HPP) is a rare inborn error of metabolism caused by mutations in the gene encoding tissue-nonspecific alkaline phosphatase gene (TNSALP), leading to low alkaline phosphatase (ALP) activity. At least 6 clinical forms of HPP have been reported. Certain benign or asymptomatic presentations of HPP in older children may remain undiagnosed, in contrast to severe perinatal and infantile types. The underlying reason of this diagnostic inconsisten...