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SUN-288 Severe Growth Hormone Deficiency in a 13-Year-Old Girl with Congenital Eye Anomalies, Secondary to Transsphenoidal Encephalocele
Background: Transphenoidal encephaloceles are very rare with estimated incidence of 1 in 700,000 live births. They can be associated with pituitary hormonal deficiencies, facial midline defects or eye anomalies. Lack of feeding problems, respiratory difficulties and/or characteristic facies can lead...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Endocrine Society
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552854/ http://dx.doi.org/10.1210/js.2019-SUN-288 |