PedAM
Pediatric Disease Annotations & Medicines
| Disease | hypopituitarism |
| Phenotype | C0013338|growth hormone deficiency |
| Sentences | 6 |
| PubMedID- 24778694 | They are often either secondary to hormonal deficiencies, including pituitary hypofunction with hypogonadism, growth hormone deficiency, hypothyroidism and abnormal glucose or insulin metabolism, or treatment-related, such as hemochromatosis with repeated transfusions, or transplant-related complications3). |
| PubMedID- 22629495 | The main reported clinical findings of sod are hypopituitarism (62–80%), with growth hormone deficiency being the commonest endocrine abnormality, visual impairment (23% having significant visual impairment), and developmental delay. |
| PubMedID- 21132537 | Detection of genetic hypopituitarism in an adult population of idiopathic pituitary insufficiency patients with growth hormone deficiency. |
| PubMedID- 20865648 | Severe growth hormone deficiency in hypopituitarism was associated with the severe degree of hepatic steatosis in nafld. |
| PubMedID- 20146168 | Objective: hypopituitarism with adult-onset growth hormone deficiency (ghd) is associated with increased cardiovascular morbidity and mortality due to premature and progressive atherosclerosis. |
| PubMedID- 25883855 | Endocrinological examinations revealed hypopituitarism with growth hormone deficiency and polyuria. |
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