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| {{Infobox Disease | | __NOTOC__ |
| | Name = Dyskeratosis congenita
| | {{Dyskeratosis congenita}} |
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| | '''For patient information, click [[Dyskeratosis congenita (patient information)|here]].''' |
| | Caption =
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| | DiseasesDB = 30105
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| | ICD10 = {{ICD10|Q|82|8|q|80}}
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| | ICD9 = {{ICD9|757.39}} | |
| | ICDO =
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| | OMIM = 305000
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| | MedlinePlus =
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| | eMedicineSubj = derm
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| | eMedicineTopic = 111
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| | MeshID = D019871
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| {{CMG}} {{AE}} {{RT}} | | {{CMG}} {{AE}} {{RT}} |
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| ==Overview== | | {{SK}} Cole-Rauschkolb-Toomey syndrome; DKCX; X-linked dyskeratosis congenita; Zinsser-Cole-Engman syndrome; Zinsser-Engman-Cole syndrome |
| '''Dyskeratosis congenita''' (DKC), also called '''Zinsser-Cole-Engman syndrome''',<ref name=omim>{{OMIM|305000}}</ref><ref name="Andrews">James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. ISBN 0-7216-2921-0.</ref>{{rp|570}} is a rare progressive [[congenital disorder]] that in some ways resembles premature aging (similar to [[progeria]]). The disease mainly affects the [[integumentary system]], the organ system that protects the body from damage, with a major consequence being anomalies of the [[bone marrow]].
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| | ==[[Dyskeratosis congenita overview|Overview]]== |
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| | ==[[Dyskeratosis congenita historical perspective|Historical Perspective]]== |
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| | ==[[Dyskeratosis congenita classification|Classification]]== |
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| | ==[[Dyskeratosis congenita pathophysiology|Pathophysiology]]== |
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| | ==[[Dyskeratosis congenita causes| Causes]]== |
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| | ==[[Dyskeratosis congenita differential diagnosis|Differentiating Dyskeratosis Congenita from other Diseases]]== |
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| | ==[[Dyskeratosis congenita epidemiology and demographics|Epidemiology and Demographics]]== |
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| | ==[[Dyskeratosis congenita risk factors|Risk Factors]]== |
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| | ==[[Dyskeratosis congenita screening|Screening]]== |
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| | ==[[Dyskeratosis congenita natural history, complications and prognosis|Natural History, Complications and Prognosis]]== |
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| | ==Diagnosis== |
| | [[Dyskeratosis congenita history and symptoms|History and Symptoms]] | [[Dyskeratosis congenita physical examination|Physical Examination]] | [[Dyskeratosis congenita laboratory findings|Laboratory Findings]] | [[Dyskeratosis congenita electrocardiogram|Electrocardiogram]] | [[Dyskeratosis congenita x ray|X Ray]] | [[Dyskeratosis congenita CT|CT]] | [[Dyskeratosis congenita MRI|MRI]] | [[Dyskeratosis congenita echocardiography or ultrasound|Echocardiography or Ultrasound]] | [[Dyskeratosis congenita other imaging findings|Other Imaging Findings]] | [[Dyskeratosis congenita other diagnostic studies|Other Diagnostic Studies]] |
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| ==Pathophysiology== | | ==Treatment== |
| Though the exact pathology of the disease is not yet fully understood, most evidence points to dyskeratosis congenita being primarily a disorder of poor [[telomere]] maintenance.<ref name="pmid11574891">{{cite journal |author=Vulliamy T, Marrone A, Goldman F, "et al." |title=The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita. |journal=Nature |volume=413 |issue=6854 |pages=432–435 |year=2001 |month=September |pmid=11574891|url=http://www.nature.com/nature/journal/v413/n6854/full/413432a0.html| doi= 10.1038/35096585}}</ref> Specifically, the disease is related to one or more mutations which directly or indirectly affect the [[vertebrate]] [[telomerase]] RNA component (TERC).
| | [[Dyskeratosis congenita medical therapy|Medical Therapy]] | [[Dyskeratosis congenita surgery|Surgery]] | [[Dyskeratosis congenita primary prevention|Primary Prevention]] | [[Dyskeratosis congenita secondary prevention|Secondary Prevention]] | [[Dyskeratosis congenita cost-effectiveness of therapy|Cost-Effectiveness of Therapy]] | [[Dyskeratosis congenita future or investigational therapies|Future or Invesetigational Therapies]] |
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| Telomerase is a [[reverse transcriptase]] which maintains a specific repeat sequence of [[DNA]], the telomere, during development. Telomeres are placed by telomerase on both ends of linear chromosomes as a way to protect linear DNA from general forms of chemical damage and to correct for the chromosomal [[Telomere#Telomere_shortening|end-shortening]] that occurs during normal [[DNA replication]].<ref name="pmid8811183">{{cite journal |author=Greider, CW. |title=Telomere length regulation. |journal=Annu. Rev. Biochem. |volume=65 |pages=337–365 |year=1996|month=May|pmid=8811183|url=http://arjournals.annualreviews.org/doi/abs/10.1146/annurev.bi.65.070196.002005?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%3dncbi.nlm.nih.gov |doi=10.1146/annurev.bi.65.070196.002005?url_ver=Z39.88-2003}}</ref> This end-shortening is the result of the eukaryotic [[DNA polymerase]]s having no mechanism for synthesizing the final [[nucleotide]]s present on the end of the "lagging strand" of double stranded DNA. DNA polymerase can only synthesize new DNA from an old DNA strand in the 5'->3' direction. Given that DNA has two strands that are complementary, one strand must be 5'->3' while the other is 3'->5'. This inability to synthesize in the 3'->5' directionality is compensated with the use of [[Okazaki fragment]]s, short pieces of DNA that are synthesized 5'->3' from the 3'->5' as the replication fork moves. As DNA polymerase requires [[Primer (molecular biology)|RNA primers]] for DNA binding in order to commence replication, each Okazaki fragment is thus preceded by an RNA primer on the strand being synthesized. When the end of the chromosome is reached, the final RNA primer is placed upon this nucleotide region, and it is inevitably removed. Unfortunately once the primer is removed, DNA polymerase is unable to synthesize the remaining bases.<ref name="pmid8811183" /><ref name="watson">{{cite book |author=Wason, James; et al. |title=Molecular Biology of the Gene. 5th ed |journal=Annu. Rev. Biochem. |publisher=San Francisco: Pearson Education, Inc|year=2004}}</ref>
| | ==Case Studies== |
| | [[Dyskeratosis congenita case study one|Case #1]] |
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| Sufferers of DKC have been shown to have a reduction in TERC levels invariably affecting the normal function of telomerase which maintains these telomeres.<ref name="pmid11574891" /><ref name="pmid17507419">{{cite journal |author=Walne AJ, Vulliamy T, Marrone A, "et al." |title=Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10. |journal=Hum Mol Genet. |volume=16 |issue=13 |pages=1619–29 |year=2007 |month=July |pmid=17507419 |url=http://hmg.oxfordjournals.org/cgi/content/full/16/13/1619 |pmc=2882227 |doi=10.1093/hmg/ddm111}}</ref><ref name="pmid9590285">{{cite journal |author=Heiss NS, Knight SW, Vulliamy TJ, "et al." |title=X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions. |journal=Nat. Genet.|volume=19 |issue=1 |pages=32–38 |year=1998 |month=May|pmid=9590285|url=http://www.nature.com/ng/journal/v19/n1/abs/ng0598-32.html| doi= 10.1038/ng0598-32}}</ref> With TERC levels down, telomere maintenance during development suffers accordingly. In humans, telomerase is inactive in most cell types after early development (except in extreme cases such as cancer).<ref name="pmid17015423">{{cite journal |author=Wong J, Collins K |title=Telomerase RNA level limits telomere maintenance in X-linked dyskeratosis congenita. |journal=Genes Dev. |volume=20 |pages=2848–2858 |year=2006 |month=October|pmid=17015423 |url=http://genesdev.cshlp.org/content/20/20/2848.long |doi=10.1101/gad.1476206 |issue=20 |pmc=1619937}}</ref> Thus, if telomerase is not able to efficiently affect the DNA in the beginning of life, chromosomal instability becomes a grave possibility in individuals much earlier than would be expected.{{fact|date=July 2012}}
| | ==External Links== |
| | * [http://www.marrowfailure.cancer.gov/index.html Dyskeratosis Congenita research study of Inherited Bone Marrow Failure Syndromes (IBMFS) ] |
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| A study shows that proliferative defects in DC skin [[keratinocytes]] are corrected by expression of the [[telomerase reverse transcriptase]], TERT, or by activation of endogenous telomerase through expression of papillomavirus E6/E7 or the telomerase [[RNA]] component, TERC. Experimental Dermatology 2010; 19: 279–288<ref>Gourronc, F. A., Robertson, M. M., Herrig, A. K., Lansdorp, P. M., Goldman, F. D. and Klingelhutz, A. J. (2010), [http://onlinelibrary.wiley.com/doi/10.1111/j.1600-0625.2009.00916.x/abstract Proliferative defects in dyskeratosis congenita skin keratinocytes are corrected by expression of the telomerase reverse transcriptase, TERT, or by activation of endogenous telomerase through expression of papillomavirus E6/E7 or the telomerase RNA component, TERC]. Experimental Dermatology, 19: 279–288. {{doi|10.1111/j.1600-0625.2009.00916.x}}</ref>
| | {{Congenital malformations and deformations of integument}} |
| | {{X-linked disorders}} |
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| ===Genetics===
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| Of the components of the telomerase RNA component (TERC), one of key importance is the [[SnoRNA#H.2FACA_box|box H/ACA]] domain. This H/ACA domain is responsible for maturation and stability of TERC and therefore of telomerase as a whole. The [[mammal]]ian H/ACA [[ribonucleoprotein]] contains four [[protein]] subunits: dyskerin, Gar1, Nop10, and Nhp2. [[Mutation]]s in Nop10,<ref name="pmid17507419" /> Nhp2<ref name="pmid18523010">{{cite journal |author=Vulliamy T, Beswick R, Kirwan M, "et al." |title=Mutations in the telomerase component Nhp2 cause the premature ageing syndrome dyskeratosis congenita. |journal=Proc Natl Acad Sci USA|volume=105 |year=2008 |month=June|pmid=18523010|url=http://www.pnas.org/content/105/23/8073.long |doi=10.1073/pnas.0800042105 |issue=23 |pages=8073–8 |pmc=2430361 }}</ref> and dyskerin1<ref name="pmid9590285" /> have all been shown to lead to DKC-like symptoms.
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| | [[Category:Disease]] |
| | [[Category:Rare diseases]] |
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| ====Autosomal recessive form====
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| The true [[phenotype]] of DKC individuals may depend upon which protein has incurred a mutation. One documented autosomal recessive mutation<ref name="pmid17507419" /> in a family that carries DKC has been found in Nop10. Specifically, the mutation is a change of base from cytosine to thymine in a highly conserved region of the Nop10 sequence. This mutation, on [[Chromosome 15 (human)|chromosome 15]], results in an [[amino acid]] change from [[arginine]] to [[tryptophan]]. [[Dominance (genetics)#Recessive trait|Homozygous recessive]] individuals show the symptoms of dyskeratosis congenita in full. As compared to age-matched normal individuals, those suffering from DKC have telomeres of a much shorter length. Furthermore, heterozygotes, those who have one normal [[allele]] and one coding for the disease, also show relatively shortened telomeres. The cause of this was determined to be a reduction in TERC levels in those with the Nop10 mutation. With TERC levels down, telomere maintenance, especially in development, would be presumed to suffer accordingly. This would lead to the telomere shortening described.<ref name="pmid17507419" />
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| Nhp2 mutations are similar in characterization to Nop10. These mutations are also autosomal recessive with three specific [[single-nucleotide polymorphism]]s being recognized which result in dyskeratosis congenita. Also like Nop10, individuals with these Nhp2 mutations have a reduction in the amount of telomerase RNA component (TERC) present in the cell. Again it can be presumed that a reduction in TERC results in aberrant telomere maintenance and thus shortened telomeres. Those homozygous recessive for mutations in Nhp2 do show shorter telomeres when compared with age-matched normal individuals.<ref name="pmid18523010" />
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| ====X-linked form====
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| The best characterized form of dyskeratosis congenita is a result of one or more mutations in the long arm of the [[X chromosome]] in the gene DKC1.<ref name="pmid11574891" /><ref name="pmid9590285" /> This results in the X-linked recessive form of the disease wherein the major protein affected is dyskerin. Of the five mutations described by Heiss and colleagues in ''Nature Genetics'',<ref name="pmid9590285" /> four were single nucleotide polymorphisms all resulting in the change of highly [[Conserved sequence|conserved amino acids]]. One case was an in-frame deletion resulting in the loss of a [[leucine]] [[amino acid|residue]], also conserved in mammals. In three of the cases, the specific amino acids affected ([[phenylalanine]], [[proline]], [[glycine]]) are found in the same [[locus (genetics)|locus]] in humans as they are in yeast (''[[S. Cerevisiae]]'') and the [[brown rat]] (''R. Norvegicus'').<ref name="pmid9590285" /> This establishes the sequence conservation and importance of dyskerin within the eukaryotes. The relevant nature of dyskerin throughout most species is to catalyze the [[RNA transcription|post-transcriptional]] [[pseudouridine|pseudouridylation]] of specific [[uridine]]s found in non-coding RNAs, such as [[ribosomal RNA]] (rRNA). Cbf5, the yeast analog of human dyskerin, is indeed known to be associated with the processing and maturation of rRNA.<ref name="pmid11574891" /> In humans this role can be attributed to dyskerin.<ref name="pmid9590285" /> Thus, the X-linked form of this disease may result in specific issues related to dysfunctional rRNA and perhaps a graver phenotype. Within the vertebrates, as opposed to single celled eukaryotes, dyskerin is a key component of the telomerase RNA component (TERC) in the form of the H/ACA motif.<ref name="pmid17015423" /> This X-linked variety, like the Nop10 and Nhp2 mutations, demonstrates shortened telomeres as a result of lower TERC concentrations.
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