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Keratolytic winter erythema(KWE)

MedGen UID:
98359
Concept ID:
C0406756
Congenital Abnormality; Disease or Syndrome
Synonyms: Erythrokeratolysis hiemalis ichthyosis; KWE; Oudtshoorn skin; OUDTSHOORN SKIN DISEASE
SNOMED CT: Oudtshoorn disease (239064000); Winter erythrokeratolysis (239064000); Erythrokeratolysis hiemalis (239064000); Keratolytic winter erythema (239064000)
Modes of inheritance:
Autosomal dominant inheritance
MedGen UID:
141047
Concept ID:
C0443147
Intellectual Product
Source: Orphanet
A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele.
 
Gene (location): CTSB (8p23.1)
 
Monarch Initiative: MONDO:0007854
OMIM®: 148370
Orphanet: ORPHA50943

Definition

Keratolytic winter erythema, also known as Oudtshoorn skin disease, manifests during childhood with recurrent episodes of palmoplantar erythema and centrifugal epidermal peeling. Lateral and dorsal aspects of the hands and feet can be involved. A less common finding is a slowly migratory, annular erythema that is seen mostly on the extremities. Between flares, the skin may appear unremarkable. Hyperhidrosis, associated with a pungent odor, is invariably present, and itching can occur. Peeling is preceded by the formation of dry blisters due to keratolysis, whereas formation of vesicles or bullae is rare. Cold weather, moisture, febrile diseases, and physical and mental stress can trigger exacerbations. In severely affected individuals, skin manifestations persist unremittingly. Penetrance of the disease is high, but expressivity is variable, even within the same family (summary by Ngcungcu et al., 2017). [from OMIM]

Clinical features

From HPO
Abnormality of the skin
MedGen UID:
11449
Concept ID:
C0037268
Congenital Abnormality
An abnormality of the skin.
Erythema
MedGen UID:
11999
Concept ID:
C0041834
Disease or Syndrome
Redness of the skin, caused by hyperemia of the capillaries in the lower layers of the skin.
Palmoplantar hyperhidrosis
MedGen UID:
224808
Concept ID:
C1274743
Disease or Syndrome
Hyperhidrosis palmaris et plantaris (HYPRPP) is characterized by excessive perspiration of the eccrine sweat gland in the palm, sole, and axilla. Perspiration in those affected may be aggravated by emotional stimuli (summary by Higashimoto et al., 2006). Stolman (1998) noted that hyperhidrosis may be complicated by skin maceration as well as secondary microbial infections, and that treatment modalities are associated with complications.

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVKeratolytic winter erythema
Follow this link to review classifications for Keratolytic winter erythema in Orphanet.

Recent clinical studies

Etiology

Schimmel RJ, Van Tuyll Van Serooskerke AM, Bladergroen RS, Van Steensel AM, van Geel M, Pasmans SG, Frank J
Cell Mol Biol (Noisy-le-grand) 2009 Jul 1;55(2):111-7. PMID: 19656459

Diagnosis

Hull PR, Hobbs A, Aron S, Ramsay M
S Afr Med J 2013 Oct 11;103(12 Suppl 1):961-5. doi: 10.7196/samj.7253. PMID: 24300638
Schimmel RJ, Van Tuyll Van Serooskerke AM, Bladergroen RS, Van Steensel AM, van Geel M, Pasmans SG, Frank J
Cell Mol Biol (Noisy-le-grand) 2009 Jul 1;55(2):111-7. PMID: 19656459
Degiovanni CV, Farrant PB, Howell S, Hull PR, Woollons A
Clin Exp Dermatol 2009 Mar;34(2):206-8. Epub 2008 Nov 6 doi: 10.1111/j.1365-2230.2008.02825.x. PMID: 19018790
Botha MC, Beighton P
S Afr Med J 1983 Oct 15;64(17):664-7. PMID: 6414096

Therapy

Degiovanni CV, Farrant PB, Howell S, Hull PR, Woollons A
Clin Exp Dermatol 2009 Mar;34(2):206-8. Epub 2008 Nov 6 doi: 10.1111/j.1365-2230.2008.02825.x. PMID: 19018790

Clinical prediction guides

Hobbs A, Aron S, Hartshorne S, Hull PR, Ramsay M
J Dermatol Sci 2012 Jan;65(1):58-62. Epub 2011 Sep 8 doi: 10.1016/j.jdermsci.2011.08.008. PMID: 21945151
Schimmel RJ, Van Tuyll Van Serooskerke AM, Bladergroen RS, Van Steensel AM, van Geel M, Pasmans SG, Frank J
Cell Mol Biol (Noisy-le-grand) 2009 Jul 1;55(2):111-7. PMID: 19656459
Danielsen AG, Weismann K, Thomsen HK
J Eur Acad Dermatol Venereol 2001 May;15(3):255-6. doi: 10.1046/j.1468-3083.2001.00258.x. PMID: 11683293
Starfield M, Hennies HC, Jung M, Jenkins T, Wienker T, Hull P, Spurdle A, Küster W, Ramsay M, Reis A
Am J Hum Genet 1997 Aug;61(2):370-8. doi: 10.1086/514848. PMID: 9311742Free PMC Article

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