Blomstrand chondrodysplasia

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Template:Blomstrand chondrodysplasia Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Syed Hassan A. Kazmi BSc, MD [2]

Overview

Blomstrand chondrodysplasia is a fatal skeletal dysplasia presenting with generalised bone sclerosis and advanced skeletal maturation. Autosomal recessive inheritance has been proposed for this disease and consanguinity increases the chances of Blomstrand chondrodysplasia in offsprings.

Differentiating Blomstrand chondrodysplasia From Other Diseases

Blonstrand chondrodysplasia should be differentiated from other causes of abnormal parathyroid hormone( PTH) and parathyroid hormone resistance such as pseudohypoparathyroidism, acrodysostosis, hypomagnesemia, hypoparathyroidism and hyperparathyroidism.[1][2][3][4]

Differential diagnosis of Pseudohypoparathyroidism
Disorders Mechanism Laboratory findings
Serum PTH Serum Calcium Serum Phosphate Other findings
Pseudohypoparathyroidism [1][2][3] Type 1a
Type 1b
Type 1c
Type 2
Pseudopseudohypoparathyroidism Normal Normal Normal --
Hypoparathyroidism
Hypomagnesemia[5][4] Inappropriately Normal/ --
Acrodysostosis Acrodysostosis type 1 Multiple hormone resistance
Acrodysostosis type 2 Multiple hormone resistance
Blomstrand chondrodysplasia Urinary Phosphate, Urinary cAMP
Hyperparathyroidism Primary hyperparathyroidism ↓/Normal Normal/↑ calcitriol
Secondary hyperparathyroidism ↓/Normal --
Tertiary hyperparathyroidism

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References

  1. 1.0 1.1 Levine MA (2012). "An update on the clinical and molecular characteristics of pseudohypoparathyroidism". Curr Opin Endocrinol Diabetes Obes. 19 (6): 443–51. doi:10.1097/MED.0b013e32835a255c. PMC 3679535. PMID 23076042.
  2. 2.0 2.1 Mantovani G (2011). "Clinical review: Pseudohypoparathyroidism: diagnosis and treatment". J. Clin. Endocrinol. Metab. 96 (10): 3020–30. doi:10.1210/jc.2011-1048. PMID 21816789.
  3. 3.0 3.1 Lee S, Mannstadt M, Guo J, Kim SM, Yi HS, Khatri A, Dean T, Okazaki M, Gardella TJ, Jüppner H (2015). "A Homozygous [Cys25]PTH(1-84) Mutation That Impairs PTH/PTHrP Receptor Activation Defines a Novel Form of Hypoparathyroidism". J. Bone Miner. Res. 30 (10): 1803–13. doi:10.1002/jbmr.2532. PMC 4580526. PMID 25891861.
  4. 4.0 4.1 Freitag JJ, Martin KJ, Conrades MB, Bellorin-Font E, Teitelbaum S, Klahr S, Slatopolsky E (1979). "Evidence for skeletal resistance to parathyroid hormone in magnesium deficiency. Studies in isolated perfused bone". J. Clin. Invest. 64 (5): 1238–44. doi:10.1172/JCI109578. PMC 371269. PMID 227929.
  5. Jahnen-Dechent W, Ketteler M (2012). "Magnesium basics". Clin Kidney J. 5 (Suppl 1): i3–i14. doi:10.1093/ndtplus/sfr163. PMC 4455825. PMID 26069819.