Vil du vite mer om syndromer?
- Acrokeratoelastoidosis
- Adams-Oliver syndrom
- Angelman syndrom
- Ascher syndrom
- Ataxia telangiektasia
- Auriculotemporal syndrom
- Barraquer-Simons syndrom
- Bazex syndrom
- Berardinelli-Seip syndrom
- Birt-Hogg-Dube syndrom
- Bloom syndrom
- Blue rubber bleb syndrom
- Blueberry muffin syndrom
- Brooke-Spiegler syndrom
- Chediak-Higashi syndrom
- CHILD syndrom
- Clouston syndrom
- Costello syndrom
- Cowden syndrom
- Degos sykdom
- Ehler-Danlos syndrom
- Ektodermale dysplasier
- Fabry sykdom
- Fokal dermal hypoplasi
- Gardner syndrom
- Gorlin syndrom
- Hay-Wells syndrom
- Howell-Evans syndrom
- Huriez syndrom
- Hypereosinofile syndromer
- Hypohidrotisk ektodermal dysplasi
- Hypomelanose av Ito
- Incontinentia pigmenti
- Keratosis follikularis spinulosa dekalvans
- Kindler syndrom
- Klippel-Trénaunay syndrom
- Kobberling-Dunningan syndrom
- Laugier Hunziker syndrom
- LEOPARD syndrom
- Lesch-Nyhan syndrom
- Linear and whorled nevoid hypermelanosis
- Macrocephaly-capillary malformation
- Marfan syndrom
- McCune-Albright syndrom
- McKusick syndrom
- Melkersson-Rosenthal syndrom
- Menke’s syndrom
- Muckle-Wells syndrom
- Muir torre syndrom
- Nail-Patella syndrom
- Naxos sykdom
- Netherton syndrom
- Olmsted’s syndrom
- Pachonychia congenita
- PAPA syndrom
- Papillon-Lefevre syndrom
- Parington kutan amyloidose
- Parry-Romberg syndrom
- Peutz-Jeghers syndrom
- POEMS syndrom
- Progeria
- Proteus syndrom
- Pseudoxantoma elastikum
- Punktat palmoplantar keratodermi
- Reed syndrom
- Reticulate acropigmentation of Kitamura
- Richner-Hanhart syndrom
- Rothmund Thomson syndrom
- SAPHO syndrom
- Schnitzler syndrom
- Sjögren-Larsson syndrom
- Trigeminal trofisk syndrom
- Trousseau syndrom
- Turner syndrom
- Vohlwinkel’s syndrom
- Witkop syndrom
- X-Linked Dominant Chondrodysplasia Punctata
- Xeroderma pigmentosus
- Yellow nail syndrom
- Zinsser-Engman-Cole syndrom
- Acrokeratoelastoidosis
- Adams-Oliver syndrom
- Angelman syndrom
- Ascher syndrom
- Ataxia telangiektasia
- Auriculotemporal syndrom
- Barraquer-Simons syndrom
- Bazex syndrom
- Berardinelli-Seip syndrom
- Birt-Hogg-Dube syndrom
- Bloom syndrom
- Blue rubber bleb syndrom
- Blueberry muffin syndrom
- Brooke-Spiegler syndrom
- Chediak-Higashi syndrom
- CHILD syndrom
- Clouston syndrom
- Costello syndrom
- Cowden syndrom
- Degos sykdom
- Ehler-Danlos syndrom
- Ektodermale dysplasier
- Fabry sykdom
- Fokal dermal hypoplasi
- Gardner syndrom
- Gorlin syndrom
- Hay-Wells syndrom
- Howell-Evans syndrom
- Huriez syndrom
- Hypereosinofile syndromer
- Hypohidrotisk ektodermal dysplasi
- Hypomelanose av Ito
- Incontinentia pigmenti
- Keratosis follikularis spinulosa dekalvans
- Kindler syndrom
- Klippel-Trénaunay syndrom
- Kobberling-Dunningan syndrom
- Laugier Hunziker syndrom
- LEOPARD syndrom
- Lesch-Nyhan syndrom
- Linear and whorled nevoid hypermelanosis
- Macrocephaly-capillary malformation
- Marfan syndrom
- McCune-Albright syndrom
- McKusick syndrom
- Melkersson-Rosenthal syndrom
- Menke’s syndrom
- Muckle-Wells syndrom
- Muir torre syndrom
- Nail-Patella syndrom
- Naxos sykdom
- Netherton syndrom
- Olmsted’s syndrom
- Pachonychia congenita
- PAPA syndrom
- Papillon-Lefevre syndrom
- Parington kutan amyloidose
- Parry-Romberg syndrom
- Peutz-Jeghers syndrom
- POEMS syndrom
- Progeria
- Proteus syndrom
- Pseudoxantoma elastikum
- Punktat palmoplantar keratodermi
- Reed syndrom
- Reticulate acropigmentation of Kitamura
- Richner-Hanhart syndrom
- Rothmund Thomson syndrom
- SAPHO syndrom
- Schnitzler syndrom
- Sjögren-Larsson syndrom
- Trigeminal trofisk syndrom
- Trousseau syndrom
- Turner syndrom
- Vohlwinkel’s syndrom
- Witkop syndrom
- X-Linked Dominant Chondrodysplasia Punctata
- Xeroderma pigmentosus
- Yellow nail syndrom
- Zinsser-Engman-Cole syndrom
Time til hudlege
Bestill time til hudlege enkelt online eller på telefon 22 03 21 00. Kort ventetid, erfarne spesialister og ingen henvisning.
Barraquer-Simons syndrom
Barraquer-Simons syndrom er en sjelden sykdom som rammer fettvev.
Symptomer
Sykdommen begynner i barnealder, og starter ofte etter en influensa liknende infeksjon. Sykdommen rammer fettvev, hvor en gradvis mister underhudsfettet. Det er beskrevet tre ulike typer. Typisk symptomer er tap av underhudsfett i den øvre delen av kroppen. Noen får paradoksalt nok økt fettvev på nedre del av kroppen. Det finnes også en sjelden varint som kun rammer den ene halvsiden. Noen har assosiert nyresykdom, og er mer utsatt for infeksjoner.
Referanser
- Dermatology: 3rd edition. Bologna JL, Jorizzo JL (Eds.). Pub: Mosby.
- Rook’s Textbook of Dermatology. Burns DA, Breathnach SM (Eds.). Pub: Wiley-Blackwell.
- Andrew’s Diseases of the skin: Clinical Dermatology. James WD, Berger TG (Eds). Pub: Saunders
- Surgery of the Skin: Procedural Dermatology. Robinson JK, Hake CW (Eds).