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Related Experiment Video

Updated: May 25, 2026

A Method to Make a Craniotomy on the Ventral Skull of Neonate Rodents
08:30

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Published on: May 22, 2014

[A neonate without claviculae].

Sybrich Tiemersma1, Martijn F Boomsma

  • 1Isala klinieken, Zwolle, Afd. Amalia kinderafdeling, the Netherlands. sybrich@gmail.com

Nederlands Tijdschrift Voor Geneeskunde
|January 20, 2012
PubMed
Summary
This summary is machine-generated.

Cleidocranial dysplasia is a rare genetic disorder affecting bone development. This case highlights key physical and radiological signs in a newborn, aiding early diagnosis.

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Area of Science:

  • Genetics
  • Pediatrics
  • Radiology

Background:

  • Cleidocranial dysplasia (CCD) is an autosomal dominant skeletal disorder.
  • It is characterized by defective ossification of the skull and clavicles.

Observation:

  • A 1-week-old infant presented with physical anomalies.
  • Observed features included short, small clavicles and widened anterior and posterior fontanelles.

Findings:

  • Radiological examination revealed hypoplastic clavicles and delayed skull ossification.
  • Maxillary hypoplasia and supernumerary teeth were also noted, consistent with CCD.

Implications:

  • Early recognition of these clinical and radiological signs is crucial for timely diagnosis of cleidocranial dysplasia.
  • This case underscores the importance of a comprehensive evaluation in neonates with skeletal abnormalities.