A neurological disorder that impairs eye movement is Parinaud's syndrome. Let's look at the characteristics of this condition, as well as diagnostic and treatment methods.
A rare disease, Proteus syndrome, is a genetic multisystem pathology with pronounced clinical manifestations, namely, selective gigantism and damage to the blood and lymphatic systems.
A rare anomaly of intrauterine body structure development, which mainly consists of hypoplasia of the sternal and costal portions of the pectoralis major muscle or its complete absence.
Goldenhar syndrome belongs to the oculo-auricular-vertebral spectrum, a group of congenital disorders of the development of structures originating from the first and second branchial (pharyngeal) arches.
Mosaic Down syndrome is a genetic disorder caused by changes in chromosome 21. Let's explore its characteristics, diagnosis, treatment, and prevention methods.
Magnetic storms can significantly impact not only human health, but also their activities – they disrupt energy systems, impair communications, and harm navigation systems.
Anterior scalene syndrome (also called Naffziger syndrome, named after the author who first described this disease – HC Naffziger, 1937) is one of the most common variants of pathology in the collective category of syndromes observed in the upper sternal entrance.
The syndrome itself is not a disease in the full sense of the word, but its symptoms indicate the development of concomitant diseases associated with impaired functioning of one or both kidneys.
