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The Zimmermann-Laband syndrome.

R A Pfeiffer1, E Seemanova, J Süss

  • 1Institut für Humangenetik, Universität Erlangen-Nürnberg.

Klinische Padiatrie
|January 1, 1992
PubMed
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Zimmermann-Laband syndrome, a rare condition, presents with gingival fibromatosis and facial swelling. This report details two cases, highlighting typical and additional features like seizures and bone abnormalities.

Area of Science:

  • Genetics and rare diseases
  • Oral and maxillofacial medicine
  • Pediatric dentistry

Background:

  • Zimmermann-Laband syndrome is a rare genetic disorder.
  • Characterized by distinctive facial and digital anomalies.

Observation:

  • Two patients presented with typical Zimmermann-Laband syndrome features.
  • Including gingival fibromatosis, perioral swelling, nail abnormalities, and terminal phalangeal defects.
  • The older patient exhibited additional symptoms: epileptic seizures, mandibular hypertrophy, mesiodentes, and lumbar spondylodysplasia.

Findings:

  • The study confirms the characteristic presentation of Zimmermann-Laband syndrome.
  • Highlights the variability and potential for additional complex manifestations.
  • Confirms early presentation of morphological features in pediatric cases.

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Implications:

  • Enhances understanding of Zimmermann-Laband syndrome's clinical spectrum.
  • Aids in early diagnosis and management of affected individuals.
  • Contributes to the literature on rare genetic disorders affecting craniofacial development.