Developments in medicine and biology in recent decades have led to a significant increase
in our knowledge of the complex interactions between the microbiota and human health. In …

Illnesses that afflict a tiny number of individuals are referred to as rare diseases (RDs),
sometimes called orphan diseases. The local healthcare systems are constantly under …

Congenital heart disease is present in over 75% of patients with Alagille syndrome. In fact,
stenosis and/or hypoplasia of the branch pulmonary arteries, the most common …

Background Matrix metalloproteinase 7 (MMP-7) is a novel biomarker for diagnosis of biliary
atresia (BA), the most common cholestatic liver disease in infancy. There is a pressing need …

Alagille syndrome (AGS) is one of the most problematic for the diagnosis of hereditary,
multisystem, cholestatic liver diseases in combination with other congenital defects. Timely …

Background Alagille syndrome (ALGS) is a rare autosomal dominant multisystem disorder
that affects the liver, heart, eyes, vertebrae, and kidneys and is associated with characteristic …

Анотація Синдром Алажиля-синдром зменшення числа міждольових жовчних протоків
або артеріопечінкова дисплазія. Генетичне мультисистемне аутосомно-домінантне …

Background: Congenital heart defect (CHD) is one of the leading causes of neonatal death.
Although the majority of CHDs are isolated, a significant number of them are associated with …

Biliary atresia (BA) is a condition of biliary obstruction. Kasai portoenterostomy (KPE) is a
treatment option. The aim to determine the success rate of kasai procedure and prognosis in …

Hội chứng Alagille (ALGS) là một rối loạn tính trội nhiễm sắc thể thường, ảnh hưởng nhiều
hệ thống cơ quan khác nhau, chủ yếu bao gồm gan, tim, mắt, cột sống và khuôn mặt …