Talk:Pseudohypoparathyroidism

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At

At 30 letters, pseudopseudohypoparathyroidism is the (or at least very close) longest actual work in the English language. As opposed to a made up word that is not actually used. Cool hu? Looktotheson 00:55, 11 April 2007 (UTC) LooktotheSon[reply]

please expand on the cAMP differences between type 2 and the others.

it mentions it but does not explain what the difference is. Thanks. 76.174.42.22 (talk) 03:04, 21 July 2008 (UTC)[reply]

Merge

Type 1A is the phenotype known as Albright Hereditary Osteodysmorphism. I highly support merging these two topics to reduce confusion.Cpt ricard (talk) 23:06, 5 July 2017 (UTC)[reply]

I support merging the article (I have consulted with and expert in the field), and also I propose to improve the definition to "Albright's hereditary osteodystrophy a form of osteodystrophy^[1], is the phenotype that can be present in patients with maternally inherited mutations in GNAS, thus pseudohypoparathyroidism 1A. But it can also be the only clinical manifestation in some patients with paternally inherited mutations, diagnosed as Pseudopseudohypoparathyroidism (PPHP)" DMzlC (talk) 11:20, 15 July 2017 (UTC)[reply]

References

^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 657. ISBN 1-4160-2999-0.

[Bolognia-1] Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 657. ISBN 1-4160-2999-0.

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