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Hyperplastic Pituitary Gland, High Serum Glycoprotein Hormone -Subunit, and Variable Circulating Thyrotropin (TSH) Levels as Hallmark of Central Hypothyroidism due to Mutations of the TSH Gene

2001; Oxford University Press; Volume: 86; Issue: 4 Linguagem: Inglês

10.1210/jc.86.4.1600

1945-7197

Marco Bonomi, Maria Carla Proverbio, Giovanna Weber, G Chiumello, Paolo Beck-Peccoz, Luca Persani,

Regulation of Appetite and Obesity

Inheritable isolated central hypothyroidism (ICH) due to mutations of TSHβ gene has been reported in few patients. For this reason the diagnostic criteria are vague. The disorder is usually characterized by undetectable TSH levels, although low/normal serum TSH, depending on TSH measurement methods, has been documented in some patients. Here we report an Egyptian girl with ICH due to a novel nonsense mutation of the TSHβ gene (Q49X). She was referred at 75 days of age for severe clinical signs of hypothyroidism, whose central origin was documented by normal serum TSH, low free T4 and free T3 levels, impaired TSH response to TRH, absence of 99Tc thyroidal uptake, and antithyroid autoantibodies. Ultrasound revealed a hypoplastic thyroid, whereas magnetic resonance imaging showed a hyperplastic pituitary. All other pituitary hormones, including PRL, were normally secreted. A diagnosis of idiopathic ICH was made, and substitutive l-T4 treatment was started at 81 days of age. At the age of 7 yr the patient had...