Long-term follow-up of a pseudohypoparathyroidism type 1A patient with missense mutation (Pro115Ser) in exon 5

J Clin Res Pediatr Endocrinol. 2010;2(2):85-8. doi: 10.4274/jcrpe.v2i2.85. Epub 2010 May 7.

Abstract

Pseudohypoparathyroidism (PHP) refers to end-organ resistance that primarily impairs the renal actions of parathyroid hormone (PTH). The patients with PHP type Ia (PHP-Ia), one of the 4 types of PHP, show resistance to other peptide hormones as well as clinical features of Albright hereditary osteodystrophy (AHO), a constellation of short stature, obesity, brachydactyly, ectopic ossifications, and/or mental retardation. Here we report clinical follow-up for a long-term period in a PHP-Ia case who had a missense mutation leading to the substitution of proline by serine (Prol115Ser) in exon 5 which has been reported previously in only two patients. An 11-year-old boy applied for hand spasm to our hospital. On physical examination, he had short stature, round-shaped face and brachydactly. Laboratory evaluation revealed PTH and TSH resistance. Molecular genetic analysis of the GNAS gene revealed a P115S substitution. The patient was followed up for 13 years. Normocalcaemia was achieved with reduced doses of calcitriol (0.25 μg/day) and calcium supplements (40 mg/kg/day). Daily requirement for levothyroxine supplementation was still high (2.3 μg/kg) to achieve euthyroidism. His pubertal development was Tanner stage V and he has no gonadotropin resistance. To our knowledge, this is the first report concerning long-term follow-up of this rare mutation. We believe that despite the genetic heterogeneity of AHO, phenotype/genotype correlations of this kind of rare mutations may help to understand progress of the disease.

Keywords: Albright’s hereditary osteodystrophy; Pseudohypoparathyroidism type Ia; mutation.

Publication types

  • Case Reports

MeSH terms

  • Calcitriol / therapeutic use
  • Child
  • Chromogranins
  • Exons / genetics*
  • Female
  • Follow-Up Studies
  • GTP-Binding Protein alpha Subunits, Gs / genetics*
  • Humans
  • Male
  • Mutation, Missense*
  • Pedigree
  • Pseudohypoparathyroidism / classification
  • Pseudohypoparathyroidism / drug therapy
  • Pseudohypoparathyroidism / genetics*
  • Time Factors
  • Vitamins / therapeutic use

Substances

  • Chromogranins
  • Vitamins
  • GNAS protein, human
  • GTP-Binding Protein alpha Subunits, Gs
  • Calcitriol