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Yin, N. Crouzon Syndrome with Acanthosis Nigricans. Encyclopedia. Available online: (accessed on 25 April 2024).
Yin N. Crouzon Syndrome with Acanthosis Nigricans. Encyclopedia. Available at: Accessed April 25, 2024.
Yin, Nicole. "Crouzon Syndrome with Acanthosis Nigricans" Encyclopedia, (accessed April 25, 2024).
Yin, N. (2020, December 24). Crouzon Syndrome with Acanthosis Nigricans. In Encyclopedia.
Yin, Nicole. "Crouzon Syndrome with Acanthosis Nigricans." Encyclopedia. Web. 24 December, 2020.
Crouzon Syndrome with Acanthosis Nigricans

Crouzon syndrome with acanthosis nigricans is a disorder characterized by the premature joining of certain bones of the skull (craniosynostosis) during development and a skin condition called acanthosis nigricans.mas.

genetic conditions

1. Introduction

The signs and symptoms of Crouzon syndrome with acanthosis nigricans overlap with those of a similar condition called Crouzon syndrome. Both conditions involve premature fusion of the skull bones, which affects the shape of the head and face. Other common features of both conditions include wide-set, bulging eyes due to shallow eye sockets; eyes that do not point in the same direction (strabismus); a small, beaked nose; and a flat or sunken appearance of the middle of the face (midface hypoplasia). Less common features that can occur in either disorder include an opening in the roof of the mouth (cleft palate), dental problems, or hearing loss. People with Crouzon syndrome or Crouzon syndrome with acanthosis nigricans usually have normal intelligence.

Crouzon syndrome with acanthosis nigricans is distinguished from Crouzon syndrome by several features, including skin abnormalities. Acanthosis nigricans is a skin condition characterized by thick, dark, velvety skin in body folds and creases, including the neck and underarms. People with Crouzon syndrome with acanthosis nigricans may also have other skin abnormalities; for example, scars in the thick, dark areas of skin are flat and pale. These scars are usually from surgical procedures that are commonly needed in affected individuals. Additionally, in some people with the condition, one or both nasal passages are narrowed (choanal stenosis) or completely blocked (choanal atresia), which can cause difficulty breathing. A buildup of fluid in the brain (hydrocephalus) can also occur. Nasal passage abnormalities and hydrocephalus are rare in Crouzon syndrome. Less common features of Crouzon syndrome with acanthosis nigricans include subtle changes in the bones of the spine (vertebrae), abnormalities of the finger bones, and noncancerous growths in the jaw called cemento

2. Frequency

Crouzon syndrome with acanthosis nigricans is rare; this condition occurs in about 1 person per million. For unknown reasons, it affects females more than twice as often as males.

3. Causes

A mutation in the FGFR3 gene causes Crouzon syndrome with acanthosis nigricans. This gene provides instructions for making a protein that is involved in the development and maintenance of bone and other tissues. The genetic change involved in this disorder causes the FGFR3 protein to be overly active, which disrupts the normal growth of skull bones and affects skin pigmentation. These changes lead to the features of Crouzon syndrome with acanthosis nigricans.

4. Inheritance

This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder.

In some cases, an affected person inherits the mutation from one affected parent. More commonly, this condition results from new (de novo) mutations in the gene. These cases occur in people with no history of the disorder in their family.

5. Other Names for This Condition

  • CAN
  • Crouzonodermoskeletal syndrome


  1. Arnaud-López L, Fragoso R, Mantilla-Capacho J, Barros-Núñez P. Crouzon withacanthosis nigricans. Further delineation of the syndrome. Clin Genet. 2007Nov;72(5):405-10.
  2. Chen F, Degnin C, Laederich M, Horton WA, Hristova K. The A391E mutationenhances FGFR3 activation in the absence of ligand. Biochim Biophys Acta. 2011Aug;1808(8):2045-50. doi: 10.1016/j.bbamem.2011.04.007.
  3. Chen F, Sarabipour S, Hristova K. Multiple consequences of a single amino acidpathogenic RTK mutation: the A391E mutation in FGFR3. PLoS One. 2013;8(2):e56521.doi: 10.1371/journal.pone.0056521.
  4. Cohen MM Jr. Let's call it "Crouzonodermoskeletal syndrome" so we won't beprisoners of our own conventional terminology. Am J Med Genet. 1999 May7;84(1):74.
  5. Mir A, Wu T, Orlow SJ. Cutaneous features of Crouzon syndrome with acanthosis nigricans. JAMA Dermatol. 2013 Jun;149(6):737-41. doi:10.1001/jamadermatol.2013.3019. Review.
  6. Schweitzer DN, Graham JM Jr, Lachman RS, Jabs EW, Okajima K, Przylepa KA,Shanske A, Chen K, Neidich JA, Wilcox WR. Subtle radiographic findings ofachondroplasia in patients with Crouzon syndrome with acanthosis nigricans due toan Ala391Glu substitution in FGFR3. Am J Med Genet. 2001 Jan 1;98(1):75-91.
  7. Vajo Z, Francomano CA, Wilkin DJ. The molecular and genetic basis offibroblast growth factor receptor 3 disorders: the achondroplasia family ofskeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome withacanthosis nigricans. Endocr Rev. 2000 Feb;21(1):23-39. Review.
  8. Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998Oct 20 [updated 2020 Apr 30]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE,Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2020. Available from
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Update Date: 24 Dec 2020