• Thumbnail for Papillon–Lefèvre syndrome
    PapillonLefèvre syndrome (PLS), also known as palmoplantar keratoderma with periodontitis, is an autosomal recessive genetic disorder caused by a deficiency...
    9 KB (969 words) - 14:54, 25 October 2024
  • demolished in 1950 Papillon Records, a British record label Papillon (name), including a list of people with the name PapillonLefèvre syndrome, a human genetic...
    3 KB (396 words) - 19:05, 3 April 2024
  • Thumbnail for Keratoderma
    keratoderma of Sybert Olmsted syndrome Naegeli–Franceschetti–Jadassohn syndrome Focal palmoplantar keratoderma PapillonLefèvre syndrome Pachyonychia congenita...
    4 KB (241 words) - 21:28, 6 June 2024
  • Pallister–Killian syndrome Panayiotopoulos syndrome Pancoast tumor Pantothenate kinase-associated neurodegeneration PAPA syndrome PapillonLefèvre syndrome Papillorenal...
    42 KB (4,068 words) - 16:56, 1 November 2024
  • Thumbnail for Cathepsin C
    "Description of two new cathepsin C gene mutations in patients with Papillon-Lefèvre syndrome". Journal of Periodontology. 77 (2): 233–7. doi:10.1902/jop.2006...
    15 KB (1,853 words) - 22:54, 2 October 2024
  • immunodeficiency syndrome) Beta-actin deficiency G-CSF-receptor deficiency Localized juvenile periodontitis PapillonLefèvre syndrome Specific granule...
    19 KB (1,836 words) - 09:52, 5 July 2024
  • language Rand RL/S, Rand Corporation's version of IBM's PL/S PapillonLefèvre syndrome, a disease affecting the teeth and skin Primary lateral sclerosis...
    2 KB (237 words) - 19:27, 1 April 2023
  • Acrokeratoelastoidosis Palmoplantar ectodermal dysplasia type 4 or PapillonLefèvre syndrome Palmoplantar ectodermal dysplasia type 5 or Tyrosinemia type II...
    2 KB (102 words) - 03:28, 22 April 2024
  • acro-osteolysis and Cochin Jewish syndrome") is a skin disease caused, like PapillonLefèvre syndrome, by a mutation in the cathepsin C gene. One of its features is...
    10 KB (1,104 words) - 02:36, 3 December 2023
  • Gougerot and Carteaud PapillonLefèvre syndrome Punctate porokeratotic keratoderma Richner–Hanhart syndrome Schöpf–Schulz–Passarge syndrome Unna Thost disease...
    13 KB (1,566 words) - 00:33, 23 August 2024
  • Thumbnail for Periodontal disease
    reduction of phagocytosis by neutrophils Ehlers–Danlos syndrome and PapillonLefèvre syndrome (also known as palmoplantar keratoderma) are also risk factors...
    76 KB (8,691 words) - 21:23, 4 November 2024
  • Panophobia Panostotic fibrous dysplasia Panthophobia Papilledema PapillonLefèvre syndrome Papillitis of the lingual papillae Papillitis of the optic nerve...
    24 KB (1,908 words) - 03:34, 11 January 2024
  • Thumbnail for List of skin conditions
    keratoderma, transgrediens and progrediens palmoplantar keratoderma) PapillonLefèvre syndrome (palmoplantar keratoderma with periodontitis) Porokeratosis plantaris...
    198 KB (17,956 words) - 10:27, 2 November 2024
  • Thumbnail for List of periodontal diseases
    neutropenia, Down syndrome, leukocyte adhesion deficiency syndromes, Papillon-Lefèvre syndrome, Chediak-Higashi syndrome, histiocytosis syndromes, glycogen storage...
    38 KB (4,054 words) - 10:27, 17 August 2024
  • Loss of deciduous and permanent teeth by late childhood PapillonLefèvre syndrome Haim–Munk syndrome Premature dentition (Natal teeth) Pachyonychia congenita...
    3 KB (160 words) - 11:27, 1 September 2024
  • syndrome Leukocyte adhesion deficiency disorder PapillonLefèvre syndrome Chédiak–Higashi syndrome Langerhans cell disease (histiocytosis syndromes)...
    5 KB (527 words) - 18:35, 29 January 2023
  • Thumbnail for Dentinogenesis imperfecta
    Kostmann's disease, cyclic neutropenia, Chediak-Hegashi syndrome, histiocytosis X, Papillon-Lefevre syndrome Permanent tooth discolouration caused by medications...
    27 KB (2,988 words) - 14:59, 14 July 2024
  • Thumbnail for Gerodermia osteodysplastica
    recessive connective tissue disorder included in the spectrum of cutis laxa syndromes. This condition is inherited in an autosomal recessive pattern and leads...
    14 KB (1,449 words) - 16:00, 10 October 2024
  • hereditary; 167800; SPINK1 Panhypopituitarism, X-linked; 312000; SOX3 PapillonLefèvre syndrome; 245000; CTSC Paraganglioma and gastric stromal sarcoma; 606864;...
    234 KB (18,877 words) - 06:16, 6 November 2024
  • 440 – keratoderma, palmoplantar, diffuse MeSH C17.800.428.435.600 – PapillonLefèvre disease MeSH C17.800.428.452 – keratosis follicularis MeSH C17.800...
    40 KB (3,128 words) - 00:03, 2 September 2024
  • 440 – keratoderma, palmoplantar, diffuse MeSH C16.320.850.475.600 – PapillonLefèvre disease MeSH C16.320.850.490 – keratosis follicularis MeSH C16.320...
    78 KB (6,496 words) - 05:23, 12 April 2022