Sjögren–Larsson syndrome

Not to be confused with Sjögren's syndrome.
Sjögren-Larsson syndrome
Classification and external resources
Specialty medical genetics
ICD-10 Q87.1 (ILDS Q87.136)
ICD-9-CM 757.1 (CDC/BPA 757.120)
OMIM 270200
DiseasesDB 30051
eMedicine derm/706
MeSH D016111
Orphanet 816

Sjögren–Larsson syndrome (SLS) is an autosomal recessive form of ichthyosis apparent at birth.[1]:485[2]:564[3] Sjögren–Larsson syndrome is a rare autosomal, recessive, neurocutaneous disease. This disease 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. The second identifier is spastic paraplegia which is characterized by leg spasms. The final identifier is intellectual delay. The gene of SLS is found on chromosome 17. In order for a child to receive SLS both parents must be carriers of the SLS gene. If they are carriers their child has a ¼ chance of getting the disease. In 1957 Sjogren and Larsson proposed that the Swedes with the disease all descended from a common ancestor 600 years ago. Today only 30-40 persons in Sweden have this disease.[4]

Causes

It is associated with a deficiency of the enzyme "fatty aldehyde dehydrogenase". At least 11 distinct mutations have been identified.[5]

Genetics

This condition is inherited in an autosomal recessive pattern.

Pathological features

Eponym

It was characterized by Torsten Sjögren and Tage Konrad Leopold Larsson (1905–1998), a Swedish medical statistician.[6][7]

It should not be confused with Sjögren's syndrome, which is a distinct condition named after a different person (Henrik Sjögren).

See also

References

  1. Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.
  2. James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
  3. Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
  4. http://www.socialstyrelsen.se/ovanligadiagnoser/sjogren-larssonssyndrom
  5. Sillén A, Anton-Lamprecht I, Braun-Quentin C, et al. (1998). "Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren-Larsson syndrome". Hum. Mutat. 12 (6): 377–84. doi:10.1002/(SICI)1098-1004(1998)12:6<377::AID-HUMU3>3.0.CO;2-I. PMID 9829906.
  6. synd/1678 at Who Named It?
  7. SJOGREN T, LARSSON T (1957). "Oligophrenia in combination with congenital ichthyosis and spastic disorders; a clinical and genetic study". Acta Psychiatr Neurol Scand Suppl 113: 1–112. PMID 13457946.

Bibliography

This article is issued from Wikipedia - version of the Sunday, January 17, 2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.