21-hydroxylase deficiency physical examination: Difference between revisions
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[[File:JCRPE-4-213-g1.jpg|thumb|none|350 px|Genital ambiguity]] | [[File:JCRPE-4-213-g1.jpg|thumb|none|350 px|Genital ambiguity]] | ||
Revision as of 14:53, 5 October 2015
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Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Microchapters |
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Differentiating Congenital adrenal hyperplasia due to 21-hydroxylase deficiency from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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21-hydroxylase deficiency physical examination On the Web |
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American Roentgen Ray Society Images of 21-hydroxylase deficiency physical examination |
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Directions to Hospitals Treating Congenital adrenal hyperplasia due to 21-hydroxylase deficiency |
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Risk calculators and risk factors for 21-hydroxylase deficiency physical examination |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ahmad Al Maradni, M.D. [2]
Overview
Patients with 21-hydroxylase deficient congenital adrenal hyperplasia usually appear underweight and dehydrated. Physical examination is usually remarkable for hypotension and virilization.
Physical Examination
Common physical examination findings of 21-hydroxylase deficient congenital adrenal hyperplasia include: [1]
Appearance
- Infants will be both underweight and dehydrated by appearance.
- Children will have tall stature, increased muscle mass, acne, and adult body odor.
Vitals
Head
Genitals
References
- ↑ Peltek Kendirci, Havva Nur et al. 'A Rare Combination: Congenital Adrenal Hyperplasia Due To 21 Hydroxylase Deficiency And Turner Syndrome. Journal of Clinical Research in Pediatric Endocrinology 4.4 (2012): 213-215. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3537289/figure/f1/