Pseudo-Crouzon Syndrome

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Classification according to ICD-10
Q75.1 Crouzon's syndrome
ICD-10 online (WHO version 2019)

The pseudo-Crouzon syndrome is a variant of the Crouzon syndrome in which there is neither a familial cluster nor a mandibular prognathy .

The first description and name was coined in 1953 by the Swiss ophthalmologist Adolphe Franceschetti (1896–1968).

The independence as a syndrome is disputed.

Individual evidence

  1. ^ Y. Samatha, TH Vardhan, AR Kiran, AJ Sankar, B. Ramakrishna: Familial Crouzon syndrome. In: Contemporary clinical dentistry. Volume 1, number 4, October 2010, pp. 277-280, doi: 10.4103 / 0976-237X.76402 , PMID 22114439 , PMC 3220155 (free full text).
  2. ↑ A. Franceschetti: dysostosis cranienne avec calotte cerebriform (pseudo-Crouzon). In: Confinia neurologica. Volume 13, Number 3, 1953, pp. 161-166, PMID 13082990 .
  3. ↑ Crouzon syndrome.  In: Online Mendelian Inheritance in Man . (English)

Web links