Congenital adrenal hyperplasia (CAH) is a rare autosomal recessive disease1 with an estimated global incidence of approximately 1 in 14,000–18,000 live births2A phase II trial has recently been ...

Table 2 Measurements of adrenal gland's stiffness and length and width. The ICC for intraobserver reliability of mean stiffness values of RAG and LAG was 0.898 (0.838–0.930) and 0.897 (0.863–0.918), ...

‌Sebaceous hyperplasia is a harmless, common skin condition that becomes more common with age. It happens when your sebaceous oil glands make too much oil that gets trapped under your skin and ...

The 4 parathyroid glands were without nodularity and pale grayish brown and bulged markedly on section. The right upper, left upper and right lower weighed 200, 140 and 350 mg. respectively.

Narrative Review Assesses Current Treatment Challenges and the Evolving Classic Congenital Adrenal Hyperplasia (CAH) Therapeutic Landscape Non-Glucocorticoid (GC) Mechanisms for Treatment of CAH Could ...

Atrophy of the contralateral adrenal gland was found in 29 per cent of the cases of adrenocortical tumors collected by Rapaport et al. 1 Several authors have postulated that prolonged hyperplasia ...

Congenital Adrenal Hyperplasia (CAH) refers to a group of genetic disorders related to adrenal gland function. These glands produce hormones that control various bodily functions. A deficiency causes ...

Summary Congenital adrenal hyperplasia (CAH) is a group of genetic conditions that hinders normal hormone levels in your adrenal glands. This causes an excess of testosterone and a lack of cortisol.

Benign prostatic hyperplasia, a noncancerous enlargement of the prostate gland, is the most common benign tumor found in men. As is true for prostate cancer, BPH occurs more often in the West than in ...

There are different types of congenital adrenal hyperplasia, including one called classic CAH. While it’s less common than the other types, it’s more serious and can be deadly if left untreated.

Approximately 95% of CAH cases are caused by a mutation that leads to deficiency of the enzyme 21-hydroxylase (21-OHD). Severe deficiency of this enzyme can lead to an inability of the adrenal glands ...