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Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
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Spirochetes, unique bacteria in the phylum Spirochaetes, are gram-negative, motile, tightly coiled, slender, and flexible. They inhabit aquatic sediments and animals, with some causing diseases like syphilis. Spirochetes are classified into eight genera based on habitat, pathogenicity, phylogeny, and characteristics.Their distinctive motility arises from endoflagella, located within the cell’s periplasm. These endoflagella anchor at the cell poles and extend along the cell length, encased by a...
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Related Experiment Video

Updated: May 29, 2026

Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome
06:48

Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome

Published on: March 23, 2022

Papillon-lefevre syndrome.

Mashkoor Ahmad1, Iffat Hassan, Qazi Masood

  • 1Department of Dermatology, STD & Leprosy, Govt. Medical College and Associated SMHS Hospital, Srinagar-Kashmir (J&K), India.

Journal of Dermatological Case Reports
|September 3, 2011
PubMed
Summary
This summary is machine-generated.

Papillon-Lefevre syndrome, a rare genetic disorder, causes severe skin and dental problems. Early diagnosis is crucial for preserving teeth in affected individuals.

Keywords:
Papillon-Lefevre syndromecathepsin Cgene mutationhyperkeratosisinfectionskeratodermaoral mucous membranespsoriasisteeth

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Area of Science:

  • Genetics
  • Dermatology
  • Dentistry

Background:

  • Papillon-Lefevre syndrome is a rare autosomal recessive disorder.
  • Caused by mutations in the cathepsin C gene, leading to deficient enzymatic activity.
  • Characterized by palmoplantar hyperkeratosis, tooth loss, and susceptibility to infections, typically starting before age 4.

Observation:

  • A 15-year-old male presented with hyperkeratosis of palms and soles, exacerbated in winter.
  • Oral examination revealed missing teeth and mobile remaining permanent teeth.
  • Gingival and labial mucosa showed fibrosis and scarring, restricting mouth opening.

Findings:

  • The patient exhibited classic symptoms of Papillon-Lefevre syndrome.
  • The late presentation highlights diagnostic challenges.
  • The case underscores the progressive nature of the syndrome's dermatological and dental manifestations.

Implications:

  • Early diagnosis of Papillon-Lefevre syndrome is vital for timely intervention.
  • Prompt treatment may help preserve dental structures and prevent further complications.
  • This case emphasizes the importance of recognizing the syndrome for improved patient outcomes.