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Long term observations in a patient with pseudohypoaldosteronism

✍ Scribed by Ronald J. Hogg; James F. Marks; Diana Marver; Jürgen C. Frolich

Publisher
Springer
Year
1991
Tongue
English
Weight
723 KB
Volume
5
Category
Article
ISSN
0931-041X

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## Abstract The 18q‐ syndrome is relatively common among cytogenetic abnormalities occurring in approximately 1 in 40,000 live births. However, interstitial deletions involving 18q12.2 to q21.1 are much less common. Only 15 cases have been reported in the literature. A phenotypic pattern is emergin