Papillon–Lefèvre 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 Papillon–Lefèvre syndrome, a human genetic...
3 KB (396 words) - 19:05, 3 April 2024
Keratoderma (redirect from Syndromic keratoderma)
keratoderma of Sybert Olmsted syndrome Naegeli–Franceschetti–Jadassohn syndrome Focal palmoplantar keratoderma Papillon–Lefèvre 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 Papillon–Lefèvre syndrome Papillorenal...
42 KB (4,068 words) - 16:56, 1 November 2024
"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 Papillon–Lefèvre 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 Papillon–Lefèvre 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 Papillon–Lefèvre 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 Papillon–Lefèvre 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 Papillon–Lefèvre syndrome Punctate porokeratotic keratoderma Richner–Hanhart syndrome Schöpf–Schulz–Passarge syndrome Unna Thost disease...
13 KB (1,566 words) - 00:33, 23 August 2024
reduction of phagocytosis by neutrophils Ehlers–Danlos syndrome and Papillon–Lefèvre 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 Papillon–Lefèvre syndrome Papillitis of the lingual papillae Papillitis of the optic nerve...
24 KB (1,908 words) - 03:34, 11 January 2024
keratoderma, transgrediens and progrediens palmoplantar keratoderma) Papillon–Lefèvre syndrome (palmoplantar keratoderma with periodontitis) Porokeratosis plantaris...
198 KB (17,956 words) - 10:27, 2 November 2024
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 Papillon–Lefèvre syndrome Haim–Munk syndrome Premature dentition (Natal teeth) Pachyonychia congenita...
3 KB (160 words) - 11:27, 1 September 2024
syndrome Leukocyte adhesion deficiency disorder Papillon–Lefèvre syndrome Chédiak–Higashi syndrome Langerhans cell disease (histiocytosis syndromes)...
5 KB (527 words) - 18:35, 29 January 2023
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
Gerodermia osteodysplastica (redirect from Martsolf Reed Hunter syndrome)
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 Papillon–Lefèvre 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 – Papillon–Lefèvre 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 – Papillon–Lefèvre disease MeSH C16.320.850.490 – keratosis follicularis MeSH C16.320...
78 KB (6,496 words) - 05:23, 12 April 2022