Limbal stem cell deficiency (LSCD) is characterized by a lack of stem cells in the limbus, which can lead to significant ocular surface issues. Althou...

Limb-girdle muscular dystrophy (LGMD) refers to a heterogeneous group of muscular dystrophies that primarily affect the muscles of the pelvic and shou...

Limb-girdle muscular dystrophy due to POMK deficiency is a genetic neuromuscular disorder that primarily affects muscle strength in the hip and should...

Limbic encephalitis is a group of autoimmune conditions marked by inflammation of the limbic system and other areas of the brain. It is most noted for...

Limbic encephalitis with caspr2 antibodies is a rare neuroimmunological disorder that primarily affects the brain’s limbic system, leading to cognitiv...

Limbic encephalitis with DPP6 antibodies is an immune-mediated condition that primarily affects the limbic system, a region of the brain that regulate...

Limbic encephalitis with LGI1 antibodies is a neuroimmunological condition that primarily affects the limbic system in the brain. It is characterized...

Limited cutaneous systemic sclerosis is a subtype of systemic sclerosis that is primarily characterized by skin fibrosis limited to the hands, face, f...

Limited dorsal myeloschisis is a rare dysraphic abnormality characterized by an abnormal, persistent connection between the neural tissue of the dorsa...

Limited systemic sclerosis is a form of systemic sclerosis characterized by organ involvement without the fibrosis typically seen in the skin. This co...

Linear and whorled nevoid hypermelanosis is a rare skin condition characterized by swirling streaks of darker skin that follow the natural lines of Bl...

Linear IgA Dermatosis is an autoimmune condition primarily affecting the skin and, in some cases, the genitourinary system. It is characterized by the...

Linear nevus sebaceous syndrome (LNSS) is a complex condition that primarily affects the skin and central nervous system, most presenting as a large s...