Growth hormone deficiency classification: Difference between revisions
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* Acquired: it may first appear in children or adults. Children with GHD present with severe growth failure, delayed bone age, delayed puberty, immature face with an underdeveloped nasal bridge, frontal bossing, sparse hair growth, and infantile fat distribution. | * Acquired: it may first appear in children or adults. Children with GHD present with severe growth failure, delayed bone age, delayed puberty, immature face with an underdeveloped nasal bridge, frontal bossing, sparse hair growth, and infantile fat distribution. | ||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
Revision as of 20:58, 16 August 2017
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Growth hormone deficiency Microchapters |
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Differentiating Growth hormone deficiency from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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Growth hormone deficiency classification On the Web |
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American Roentgen Ray Society Images of Growth hormone deficiency classification |
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Risk calculators and risk factors for Growth hormone deficiency classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Classification
Growth hormone deficiency can be classified by nature into:
- Congenital: infants may show symptoms from the first day but some patients wait until 6 months to show symptoms. Hypoglycemia, neonatal growth failure, neonatal jaundice, and asphyxia are common in these cases. The combination of GHD with gonadotropin deficiency can cause microphallus, cryptorchidism, and severe hypoglycemia.
- Acquired: it may first appear in children or adults. Children with GHD present with severe growth failure, delayed bone age, delayed puberty, immature face with an underdeveloped nasal bridge, frontal bossing, sparse hair growth, and infantile fat distribution.