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Bone Abstracts (2017) 6 P043 | DOI: 10.1530/boneabs.6.P043

1Children’s Hospital P.A. Kyriakou, Athens, Greece; 2Faculty of Medicine Univ of Southampton, Southhampton, UK; 3INSERM, Paris, France.

Background: Hypocalcemia presenting in adolescence is rare. Most common etiology is autoimmune hypoparathyroidism. Pseudohypoparathyroidism (PHP) is a rare group of disorders characterized by end-organ resistance to parathyroid hormone (PTH), and other hormones, such as TSH, with or without features of Albright’s hereditary osteodystrophy.

Case presentation: A 14-year-old boy presented complaining of fatigue and spontaneous carpal spasms in association with a febrile viral illness. Past medical history was significant for an episode of asymptomatic hypocalcemia treated with calcium and alphacalcidol. He had discontinued therapy and he was lost to follow-up. Family history was remarkable for episodes of hand numbness for the mother, muscle cramps for maternal grandfather and carpal spasms and multiple fractures for maternal great grand mother. Physical examination revealed an adolescent with no dysmorphic features, normal height and weight, fully pubertal, with no skeletal abnormalities except for mild genu valgum. He had positive Chvostek and Trousseau sign. Laboratory investigation revealed markedly low serum calcium (5.3 mg/dl), phosphate (5.6 mg/dl), magnesium, albumin ALP and TSH were normal. PTH was markedly elevated (299.4 pg/ml). and he had vitamin D deficiency(16.5 μg/lt). ECG showed prolonged corrected QT interval. The patient was initially treated with calcium and alphacalcidol. In summary, this patient presented with PTH resistance, and no phenotypic signs of Albright’s osteodystrophy, normal puberty, thyroid function and cortisol production, consistent with the diagnosis of PHP-I. A molecular genetic analysis was performed that revealed loss of methylation at the GNAS locus consistent with the diagnosis of PHP type Ib.

Conclusion: PHP-Ib is the result of defects in the methylation pattern of the complex GNAS locus and it can be inherited in an autosomal-dominant manner or may occur sporadically. The human GNAS gene is located on chromosome 20q13 and defects are heterogeneous. Genetic counselling is important for the patient and the family, as well as the need for life-long treatment with calcium and activated vitamin D.

Disclosure: The authors declared no competing interests.

Volume 6

8th International Conference on Children's Bone Health


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