sjögren larsson syndrome wiki - Axtarish в Google
Sjögren–Larsson syndrome is a rare autosomal recessive form of ichthyosis with neurological symptoms . It can be identified by a triad of medical disorders. The first is ichthyosis, which is a buildup of skin to form a scale-like covering that causes dry skin and other problems.
Sjögren's disease (SjD) is a long-term autoimmune disease that primarily affects the body's exocrine glands, particularly the lacrimal and salivary glands. Henrik Sjögren · Dry eye syndrome · Slađana Milošević · Cryoglobulinemia
9 мая 2019 г. · Sjögren-Larsson syndrome (SLS) is an inherited disorder characterized by scaling skin (ichthyosis), intellectual disability, speech ...
1 окт. 2011 г. · Sjögren-Larsson syndrome is a condition characterized by dry, scaly skin (ichthyosis); neurological problems; and eye problems.
A rare neurocutaneous disorder caused by an inborn error of lipid metabolism and characterized by congenital ichthyosis, intellectual deficit, and spasticity.
7 янв. 2020 г. · Sjogren Larsson syndrome is characterized by the triad of ichthyosis, mental retardation and spastic diplegia. The onset is during infancy or ...
autosomal recessive disease · neurometabolic disease · disorder of phospholipids, sphingolipids and fatty acids biosynthesis with central nervous system ...
Sjögren-Larsson syndrome is a rare inherited disorder that affects the skin and nervous system. The most common symptoms and signs are variable degrees.
The disorder is characterized by dry, scaly skin, neurological problems, and eye problems that can appear in early childhood. What Are the Symptoms? Symptoms of ...
Sjögren‐Larsson syndrome (SLS) is a rare inborn error of lipid metabolism. The syndrome is caused by mutations in the ALDH3A2 gene.
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