Sentence examples for permanent insufficiency from inspiring English sources

Exact(1)

To summarize, with long-term follow-up we found that temporary K-wire or screw stabilization of acute grade-V AC joint dislocation achieved good functional outcome, and that the sequelae were of minor importance and did not lead to any permanent insufficiency.

Similar(56)

One patient in our current study developed a disabling neurological condition and permanent hormonal insufficiency following acute NE.

Although self-limiting in most cases, postcontrast AKI carries a risk of more permanent renal insufficiency, dialysis, and death [ 29].

Although self-limiting in most cases, postcontrast AKI carries a risk of more permanent renal insufficiency, dialysis, and death.

He developed permanent pituitary insufficiency and also, he developed a prolonged cognitive impairment and severe neuralgia on the left side of his head.

The permanent effects of TH insufficiency on neurologic development were discussed above.

A recent report described two cousins with a homozygous hypomorphic PDX1 mutation causing permanent neonatal diabetes with subclinical exocrine insufficiency.

Subsequently, two cousins with permanent neonatal diabetes and subclinical exocrine insufficiency were reported 9. We report a further four cases with biallelic PDX1 mutations without clinical evidence of exocrine pancreatic insufficiency.

Null mutations that abolish the protein activity cause pancreatic agenesis, while hypomorphic mutations partially affecting the protein functionality lead to permanent neonatal diabetes with or without exocrine insufficiency.

Differently from adults, who most likely can recover from transient hypothyroidism without permanent health consequences, a short period of TH insufficiency may produce permanent neurologic deficits in children (Van Vliet 1999).

Recently, Nicolino et al. 9 reported a family where two cousins with permanent neonatal diabetes and no clinical sign of pancreatic insufficiency harboured a homozygous missense mutation in PDX1 (E178G).

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