Persistent hypercalcaemia in trisomy 21: consider ABCD syndrome

Elisabeth Laurer; Alexandra Blaschitz; Marlene Wimleitner; Thomas Hörtenhuber; Wolfgang Högler; Rodrigo Montero-Lopez; Julian Schirl

doi:10.1530/endoabs.110.P281

Persistent hypercalcaemia in trisomy 21: consider ABCD syndrome

^*Corresponding author for this work

Department of Pediatrics and Adolescent Medicine

Research output: Chapter in Book/Report/Conference proceeding › Poster › peer-review

Original language	English
Title of host publication	Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025: Connecting Endocrinology Across the Life Course
Edition	1
DOIs	https://doi.org/10.1530/endoabs.110.P281
Publication status	Published - 2025

Publication series

Name	Endocrine Abstracts
ISSN (Print)	1470-3947
ISSN (Electronic)	1479-6848

Fields of science

302035 Paediatrics and adolescent medicine

Access to Document

10.1530/endoabs.110.P281

Cite this

Laurer, E., Blaschitz, A., Wimleitner, M., Hörtenhuber, T., Högler, W., Montero-Lopez, R., & Schirl, J. (2025). Persistent hypercalcaemia in trisomy 21: consider ABCD syndrome. In Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025: Connecting Endocrinology Across the Life Course (1 ed.). (Endocrine Abstracts). https://doi.org/10.1530/endoabs.110.P281

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title = "Persistent hypercalcaemia in trisomy 21: consider ABCD syndrome",

author = "Elisabeth Laurer and Alexandra Blaschitz and Marlene Wimleitner and Thomas H{\"o}rtenhuber and Wolfgang H{\"o}gler and Rodrigo Montero-Lopez and Julian Schirl",

year = "2025",

doi = "10.1530/endoabs.110.P281",

language = "English",

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Laurer, E , Blaschitz, A , Wimleitner, M , Hörtenhuber, T , Högler, W , Montero-Lopez, R & Schirl, J 2025, Persistent hypercalcaemia in trisomy 21: consider ABCD syndrome. in Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025: Connecting Endocrinology Across the Life Course. 1 edn, Endocrine Abstracts. https://doi.org/10.1530/endoabs.110.P281

Persistent hypercalcaemia in trisomy 21: consider ABCD syndrome. / Laurer, Elisabeth ; Blaschitz, Alexandra ; Wimleitner, Marlene et al.
Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025: Connecting Endocrinology Across the Life Course. 1. ed. 2025. (Endocrine Abstracts).

Research output: Chapter in Book/Report/Conference proceeding › Poster › peer-review

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T1 - Persistent hypercalcaemia in trisomy 21: consider ABCD syndrome

AU - Laurer, Elisabeth

AU - Blaschitz, Alexandra

AU - Wimleitner, Marlene

AU - Hörtenhuber, Thomas

AU - Högler, Wolfgang

AU - Montero-Lopez, Rodrigo

AU - Schirl, Julian

PY - 2025

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DO - 10.1530/endoabs.110.P281

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Laurer E , Blaschitz A , Wimleitner M , Hörtenhuber T , Högler W , Montero-Lopez R et al. Persistent hypercalcaemia in trisomy 21: consider ABCD syndrome. In Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025: Connecting Endocrinology Across the Life Course. 1 ed. 2025. (Endocrine Abstracts). doi: 10.1530/endoabs.110.P281