Sjögren-Larsson syndrome
Rud's syndrome

Sjögren-Larsson syndrome is named for him (along with Tage Larsson).

The metabolism of these compounds is impaired in several inherited human peroxisomal disorders, including adrenoleukodystrophy and Sjögren-Larsson syndrome.

The disorder should not be confused with the Sjögren-Larsson syndrome, which was also denoted T. Sjögren syndrome in early studies.

Long-chain-aldehyde dehydrogenase (or fatty aldehyde dehydrogenase) is an aldehyde dehydrogenase enzyme associated with Sjögren-Larsson syndrome.

Henrik Sjögren should not be confused with his contemporary, Torsten Sjögren, for whom is named the Sjögren-Larsson syndrome (along with Tage Larsson).

Ichthyosis, Spastic Neurologic Disorder, Mental Retardation SLS None Sjögren-Larsson syndrome is an inherited disorder characterized by scaling skin (ichthyosis), mental retardation, speech abnormalities, and spasticity.

Less well documented causes include Sjögren-Larsson syndrome, Netherton syndrome, Gaucher disease type 2, congenital hypothyroidism, Conradi syndrome, Dorfman-Chanarin syndrome, ketoadipiaciduria, koraxitrachitic syndrome, ichthyosis variegata and palmoplantar keratoderma with anogenital leukokeratosis.

Rud syndrome (also known as "Rud's syndrome") is a poorly characterized disorder, probably of recessive inheritance, that includes epilepsy, mental retardation, infantilism, congenital ichthyosis, and retinitis pigmentosa.