Searchable abstracts of presentations at key conferences in endocrinology

ea0065p111 | Bone and calcium | SFEBES2019

Hypophosphatasia in an infant: a differential diagnosis that should not be overlooked

Toellner Hannah , Chong Zhuo Min , Srivastava Rajeev , McNeilly Jane , Koppel David , Sangra Meharpal , Shaikh Guftar , McDevitt Helen , Mason Avril , Kinning Esther , Ahmed Syed Faisal

Introduction: Hypophosphatasia is a very rare inherited condition due to ALPL variants and is associated with a variable presentation.Case description: The index case initially presented at 7 months with bulging anterior fontanelle, failure to thrive and mild developmental delay. She was born at 34 weeks gestation and had amniotic bands causing digital anomalies. She was sitting at 8 months, crawling by 15 months and a hearing test was normal. A...