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Related Experiment Video

Updated: May 20, 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

Zimmermann-Laband syndrome: a case report.

K Sawaki1, K Mishima, A Sato

  • 1Department of Dentistry and Oral Surgery, Hiroshima City Hospital, Japan.

The Journal of Clinical Pediatric Dentistry
|July 31, 2012
PubMed
Summary
This summary is machine-generated.

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Zimmermann-Laband syndrome, a rare genetic disorder, presents with distinct physical anomalies. This report details an unusual newborn case, highlighting early-onset symptoms of this rare condition.

Area of Science:

  • Genetics
  • Pediatrics
  • Rare Diseases

Background:

  • Zimmermann-Laband syndrome is a rare disorder.
  • It is characterized by gingival fibromatosis, cartilage abnormalities, nail/phalange hypoplasia, joint hypermobility, hepatosplenomegaly, hirsutism, and learning difficulties.
  • Early-onset presentations in newborns are infrequently documented.

Related Experiment Videos

Last Updated: May 20, 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