The Sjogren-Larsson syndrome is sometimes called the T. Sjogren syndrome to distinguish it from the sicca syndrome, which was described by Henrick Sjogren, a Swedish ophthalmologist.
Also known as the Sjogren-Larsson syndrome, this is a genetic (inherited) disease usually characterized by a triad of clinical findings consisting of ichthyosis (thickened fish-like skin), ...
FAO deficiency (aka Sjogren-Larsson syndrome): A genetic (inherited) disease usually characterized by a triad of clinical findings consisting of ichthyosis (thickened fish-like skin), ...
Raynaud's phenomenon, a disorder that affects the arteries of the arms and legs
skin diseases, such as psoriasis
endocrine disorders, such as Sjogren-Larsson syndrome, which also causes dry skin
malnutrition ...
peeling skin syndrome
pityriasis rubra pilaris (PRP)
Refsum's disease (phytanic acid storage disease)
Rud's syndrome
Sjogren-Larsson syndrome
Tay's syndrome (trichothiodystrophy, IBIDS syndrome)
X-linked ichthyosis ...
 See also: Symptom, Deficiency, Ichthyosis, Spastic paraplegia, Paraplegia
  
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