Mucolipidosis is a group of inherited metabolic disorders that affect the body's ability to carry out the normal turnover of various materials within cells. [1] When originally named, the …

What is mucolipidosis II (ML II)? Mucolipidosis II (ML II) is a rare, inherited disorder that is progressive in nature and affects many of the body’s systems. Mucolipidosis II is also known …

Mucolipidoses (MLs) are classified as a lysosomal storage diseases (LSDs) because of their involvement in increased storage materials in the lysosomes. Around 50 LSDs have been …

Mucolipidosis type II (ML II), also known as I cell disease, is a rare and progressive metabolic disorder that involves our body's ability to break down certain fats (mucolipids). Symptoms …

Mucolipidosis II alpha/beta (also known as I-cell disease) is a progressively debilitating disorder that affects many parts of the body. Explore symptoms, inheritance, genetics of this condition.

What is Mucolipidosis I (ML I)? Mucolipidosis I (ML I) is a rare, inherited disorder. Mucolipidosis I is also known as sialidosis. The condition is classified as a lysosomal storage disorder (LSD). …

Mucolipidosis type IV is an inherited disorder characterized by delayed development and vision impairment that worsens over time. The severe form of the disorder is called typical …

Mucolipidosis III (ML III) is a rare, inherited disorder that is progressive in nature and affects many of the body’s systems. It is one of many diseases classified as a lysosomal storage disorder …

2005年1月28日 · Mucolipidosis IV (MLIV) is an ultra-rare lysosomal storage disorder characterized by severe psychomotor delay, progressive visual impairment, and achlorhydria.

2015年8月11日 · Mucolipidosis IV is a rare metabolic disorder characterized by intellectual disability; severe impairment in the acquisition of skills requiring the coordination of muscular …