Periodontitis, Aggressive, 1

Description

Aggressive periodontitis, which may be generalized or localized, is characterized by severe and protracted gingival infections, leading to tooth loss. Amounts of microbial deposits are generally inconsistent with the severity of periodontal tissue destruction and the progression of attachment and bone loss may be self arresting (American Academy of Periodontology, 2000). The term 'aggressive periodontitis' replaced the terms 'early-onset,' 'prepubertal,' or 'juvenile periodontitis' at a 1999 International workshop for a classification of periodontal disease and conditions, where it was decided that the classification terminology should not be age dependent or require knowledge of rates of progression (Armitage, 1999). Genetic Heterogeneity of Aggressive PeriodontitisAggressive periodontitis-2 (OMIM ) has been mapped to chromosome 1q25.

Clinical Features

Phenotypes and symptoms related to Periodontitis, Aggressive, 1

  • Abnormality of the skin
  • Premature loss of teeth
  • Periodontitis
  • Gingival recession
  • Severe periodontitis

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— The onset for some of the known clinical features related to this disease may vary, including infantile onset .

Alternative names

Periodontitis, Aggressive, 1 Is also known as jp, periodontitis, prepubertal, ppp, jpd, periodontitis, juvenile.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Periodontitis, Aggressive, 1 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Lysosomal Storage Disease Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).

SGSH, SLC17A5, SMPD1, TCF4, MCOLN1, NPC2, ADAMTSL2, DNAJC5, SUMF1, TPP1, CLN3, CLN5, CLN6, CLN8, DYM, ANTXR2, COL11A2, PEX26, GNE, CTNS , (...)

View the complete list with 54 more genes
Specificity
2 %
Genes
100 %
CTSC.

By Institute for Human Genetics University Clinic Freiburg (Germany).

CTSC
Specificity
100 %
Genes
100 %
CTSC. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).

CTSC
Specificity
100 %
Genes
100 %
Papillon-Lefevre syndrome (sequence analysis of CTSC gene).

By CGC Genetics (Portugal).

CTSC
Specificity
100 %
Genes
100 %
Haim-Munk syndrome (sequence analysis of CTSC gene).

By CGC Genetics (Portugal).

CTSC
Specificity
100 %
Genes
100 %
Papillon-Lefevre Syndrome (PLS) via CTSC Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

CTSC
Specificity
100 %
Genes
100 %
Haim-Munk syndrome.

By Centogene AG - the Rare Disease Company (Germany).

CTSC
Specificity
100 %
Genes
100 %
Papillon-Lefevre syndrome.

By Centogene AG - the Rare Disease Company (Germany).

CTSC
Specificity
100 %
Genes
100 %

You can get up to 20 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM Genetic Syndrome Finder

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