Albright's hereditary osteodystrophy

This article is about the subtype of pseudohypoparathyroidism known as Albright's hereditary osteodystrophy. For the genetically-related condition, see McCune–Albright syndrome.
Albright's hereditary osteodystrophy
Albright's hereditary osteodystrophy has an autosomal dominant pattern of inheritance
SpecialtyEndocrinology 
SymptomsChoroid plexus calcification, Full cheeks[1]
CausesGs alpha subunit deficiency[2]
Diagnostic methodcalcium, phosphorus, PTH, Urine test for phosphorus and cyclic AMP
TreatmentPhosphate binders, supplementary calcium [3]
Named afterFuller Albright

Albright's hereditary osteodystrophy is a form of osteodystrophy,[4] and is classified as the phenotype of pseudohypoparathyroidism type 1A; this is a condition in which the body does not respond to parathyroid hormone.[1]

  1. ^ a b "Albright's hereditary osteodystrophy". Genetic and Rare Diseases Information Center (GARD) – an NCATS Program. Archived from the original on 11 February 2017. Retrieved 9 February 2017.
  2. ^ Cite error: The named reference or was invoked but never defined (see the help page).
  3. ^ Cite error: The named reference nel was invoked but never defined (see the help page).
  4. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 657. ISBN 978-1-4160-2999-1.
This article is issued from Wikipedia. The text is available under Creative Commons Attribution-Share Alike 4.0 unless otherwise noted. Additional terms may apply for the media files.