17 alpha-hydroxylase deficiency is a rare congenital adrenal hyperplasia resulting from inactivating mutations in the CYP17A1 gene. This enzyme deficiency disrupts steroidogenesis by impairing ...

Alpha-1 Antitrypsin Deficiency And Related Disorders Publication Trend The graph below shows the total number of publications each year in Alpha-1 Antitrypsin Deficiency And Related Disorders.

Alpha-1-antitrypsin is a so-called protease inhibitor, a type of enzyme inhibitor. It is produced in the liver but exerts its effects in the lungs, where it regulates immune cell activity. This ...

About congenital adrenal hyperplasia Classic CAH is a rare, autosomal recessive disorder 1 affecting 1 in 14,000–18,000 live births worldwide. 2 Classic CAH is characterized by an enzyme deficiency, ...

PetMed Express Receives Notification of Deficiency from Nasdaq Related to Delayed Filing of Annual Report on Form 10-K ...

Lundbeck today announces that orphan drug designation has been granted to Lu AG13909 by the US Food and Drug Administration (FDA) on 12 May 2025 and the European Medicines Agency (EMA) on 20 June ...

Acclaimed program of ideas, in-depth analysis, and commentary on a variety of matters—political, economic, social, and cultural—important to progressive and radical thinking and activism. Against the ...

A high-level overview of Summit Therapeutics Inc. (SMMT) stock. View (SMMT) real-time stock price, chart, news, analysis, analyst reviews and more.

Relative Energy Deficiency in Sport (REDs) was first introduced in 2014 by the International Olympic Committee’s expert writing panel, identifying a syndrome of deleterious health and performance ...