U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome(KLICK)

MedGen UID:
356430
Concept ID:
C1866029
Disease or Syndrome
Synonyms: Keratosis linearis with ichthyosis congenita and sclerosing keratoderma; KLICK SYNDROME
SNOMED CT: KLICK syndrome (763775000); Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome (763775000)
Modes of inheritance:
Autosomal recessive inheritance
MedGen UID:
141025
Concept ID:
C0441748
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 individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele).
 
Gene (location): POMP (13q12.3)
 
Monarch Initiative: MONDO:0011169
OMIM®: 601952
Orphanet: ORPHA281201

Definition

Keratosis linearis with ichthyosis congenita and sclerosing keratoderma (KLICK) is an autosomal recessive disorder of keratinization characterized by ichthyosis, palmoplantar keratoderma with constricting bands around fingers, flexural deformities of fingers, and keratotic papules in a linear distribution on the flexural side of large joints. Histologic examination shows hypertrophy and hyperplasia of the spinous, granular, and horny epidermal layers, with abundant abnormal keratohyaline granules in differentiated keratinocytes (summary by Dahlqvist et al., 2010). [from OMIM]

Clinical features

From HPO
Honeycomb palmoplantar hyperkeratosis
MedGen UID:
1787619
Concept ID:
C5539406
Disease or Syndrome
Abnormal thickening of the skin on the palms and soles with an honeycomb pattern.
Ichthyosis
MedGen UID:
7002
Concept ID:
C0020757
Disease or Syndrome
An abnormality of the skin characterized the presence of excessive amounts of dry surface scales on the skin resulting from an abnormality of keratinization.
Parakeratosis
MedGen UID:
10572
Concept ID:
C0030436
Disease or Syndrome
Abnormal formation of the keratinocytes of the epidermis characterized by persistence of nuclei, incomplete formation of keratin, and moistness and swelling of the keratinocytes.
Congenital nonbullous ichthyosiform erythroderma
MedGen UID:
38180
Concept ID:
C0079154
Disease or Syndrome
The term collodion baby applies to newborns who appear to have an extra layer of skin (known as a collodion membrane) that has a collodion-like quality. It is a descriptive term, not a specific diagnosis or disorder (as such, it is a syndrome). Affected babies are born in a collodion membrane, a shiny waxy outer layer to the skin. This is shed 10-14 days after birth, revealing the main symptom of the disease, extensive scaling of the skin caused by hyperkeratosis. With increasing age, the scaling tends to be concentrated around joints in areas such as the groin, the armpits, the inside of the elbow and the neck. The scales often tile the skin and may resemble fish scales.
Nail dystrophy
MedGen UID:
66368
Concept ID:
C0221260
Disease or Syndrome
Onychodystrophy (nail dystrophy) refers to nail changes apart from changes of the color (nail dyschromia) and involves partial or complete disruption of the various keratinous layers of the nail plate.
Hyperconvex nail
MedGen UID:
488894
Concept ID:
C0423807
Finding
When viewed on end (with the digit tip pointing toward the examiner's eye) the curve of the nail forms a tighter curve of convexity.
Linear arrays of macular hyperkeratoses in flexural areas
MedGen UID:
355608
Concept ID:
C1866031
Finding
Amniotic constriction ring
MedGen UID:
315953
Concept ID:
C1527388
Congenital Abnormality
Annular constrictions around the digits, limbs, or trunk, occurring congenitally (sometimes causing intrauterine autoamputation) and also associated with a wide variety of disorders. Constrictive amniotic bands are the result of primary amniotic rupture, which can lead to entanglement of fetal tissue (especially limbs) in fibrous amniotic strands.

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVKeratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome
Follow this link to review classifications for Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome in Orphanet.

Professional guidelines

PubMed

Thomas BR, O'Toole EA
Acta Derm Venereol 2020 Mar 25;100(7):adv00094. doi: 10.2340/00015555-3430. PMID: 32147745Free PMC Article
Guerra L, Diociaiuti A, El Hachem M, Castiglia D, Zambruno G
Orphanet J Rare Dis 2015 Sep 17;10:115. doi: 10.1186/s13023-015-0336-4. PMID: 26381864Free PMC Article
el Darouti MA, Al Raubaie SM, Eiada MA
Int J Dermatol 1988 Jan-Feb;27(1):63-6. doi: 10.1111/j.1365-4362.1988.tb02344.x. PMID: 2964426

Recent clinical studies

Etiology

Thomas BR, O'Toole EA
Acta Derm Venereol 2020 Mar 25;100(7):adv00094. doi: 10.2340/00015555-3430. PMID: 32147745Free PMC Article
Uitto J, Youssefian L, Saeidian AH, Vahidnezhad H
Acta Derm Venereol 2020 Mar 25;100(7):adv00095. doi: 10.2340/00015555-3431. PMID: 32147742Free PMC Article
Has C, Technau-Hafsi K
J Dtsch Dermatol Ges 2016 Feb;14(2):123-39; quiz 140. doi: 10.1111/ddg.12930. PMID: 26819106
Ramos-E-Silva M, Carvalho JC, Carneiro SC
Clin Dermatol 2011 Sep-Oct;29(5):541-7. doi: 10.1016/j.clindermatol.2010.09.022. PMID: 21855730
Landow RK, Cheung H, Bauer M
Int J Dermatol 1983 Apr;22(3):177-9. doi: 10.1111/j.1365-4362.1983.tb03359.x. PMID: 6222004

Diagnosis

Huang YY, Li JH
JAMA Dermatol 2024 Feb 1;160(2):218-219. doi: 10.1001/jamadermatol.2023.4152. PMID: 38055272
Al-Hamdi KI, Qais Saadoon A, Abduljabbar NH
JAMA Dermatol 2020 Oct 1;156(10):1126. doi: 10.1001/jamadermatol.2020.2555. PMID: 32745176
Thomas BR, O'Toole EA
Acta Derm Venereol 2020 Mar 25;100(7):adv00094. doi: 10.2340/00015555-3430. PMID: 32147745Free PMC Article
Adhisivam B, Mahadevan S
Indian J Pediatr 2006 Apr;73(4):359-60. doi: 10.1007/BF02825834. PMID: 16816500
Fonseca E, Peña C, Del Pozo J, Almagro M, Yebra MT, Cuevas J, Contreras F
J Cutan Pathol 2001 May;28(5):271-5. doi: 10.1034/j.1600-0560.2001.028005271.x. PMID: 11401671

Therapy

Marukian NV, Levinsohn JL, Craiglow BG, Milstone LM, Choate KA
Pediatr Dermatol 2017 Mar;34(2):160-162. Epub 2016 Dec 23 doi: 10.1111/pde.13057. PMID: 28008647
Nguyen RH, Nuara AA, Suwattee P, Cockerell CJ, Pandya AG
Am J Dermatopathol 2013 Jun;35(4):494-5. doi: 10.1097/DAD.0b013e31827654ae. PMID: 23689695
Ali ME, Sikdar AU, Akhtar N, Islam ZM
Mymensingh Med J 2007 Jan;16(1):100-3. doi: 10.3329/mmj.v16i1.262. PMID: 17344790
Dhadke SV, Kulkarni PM, Dhadke VN, Deshpande NS, Wattamwar PR
J Assoc Physicians India 2006 Mar;54:246-7. PMID: 16800355
Thiers BH
J Am Acad Dermatol 1997 Sep;37(3 Pt 2):S69-71. PMID: 9344189

Prognosis

Polivka L, Bodemer C, Hadj-Rabia S
J Med Genet 2016 May;53(5):289-95. Epub 2015 Sep 23 doi: 10.1136/jmedgenet-2015-103403. PMID: 26399581
Ramos-E-Silva M, Carvalho JC, Carneiro SC
Clin Dermatol 2011 Sep-Oct;29(5):541-7. doi: 10.1016/j.clindermatol.2010.09.022. PMID: 21855730
Robertson EV, Jankowski JA
Am J Gastroenterol 2008 Feb;103(2):443-9. Epub 2007 Oct 9 doi: 10.1111/j.1572-0241.2007.01574.x. PMID: 17925001
Adhisivam B, Mahadevan S
Indian J Pediatr 2006 Apr;73(4):359-60. doi: 10.1007/BF02825834. PMID: 16816500
Armstrong AP, Percival N
J R Soc Med 1997 Feb;90(2):81-2. doi: 10.1177/014107689709000208. PMID: 9068437Free PMC Article

Clinical prediction guides

Shirahama T, Hamada T, Abe T, Arakawa M, Teye K, Koga H, Ishii N, Nakama T
J Dermatol 2022 Aug;49(8):783-786. Epub 2022 Apr 25 doi: 10.1111/1346-8138.16405. PMID: 35467044
Vink CP, Ockeloen CW, ten Kate S, Koolen DA, Ploos van Amstel JK, Kuijpers-Jagtman AM, van Heumen CC, Kleefstra T, Carels CE
Eur J Hum Genet 2014 Sep;22(9):1063-70. Epub 2014 Jan 8 doi: 10.1038/ejhg.2013.300. PMID: 24398796Free PMC Article
Fonseca E, Peña C, Del Pozo J, Almagro M, Yebra MT, Cuevas J, Contreras F
J Cutan Pathol 2001 May;28(5):271-5. doi: 10.1034/j.1600-0560.2001.028005271.x. PMID: 11401671
Verma KC, Chaddha MK, Joshi RK
Int J Dermatol 1979 Mar;18(2):146-9. doi: 10.1111/j.1365-4362.1979.tb04493.x. PMID: 154478
Umbert P, Belcher RW, Winkelmann RK
Br J Dermatol 1976 Nov;95(5):475-80. doi: 10.1111/j.1365-2133.1976.tb00856.x. PMID: 136265

Recent systematic reviews

Polivka L, Bodemer C, Hadj-Rabia S
J Med Genet 2016 May;53(5):289-95. Epub 2015 Sep 23 doi: 10.1136/jmedgenet-2015-103403. PMID: 26399581

Supplemental Content

Table of contents

    Clinical resources

    Practice guidelines

    • PubMed
      See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...