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  2. Crouzon syndrome - Wikipedia

    en.wikipedia.org/wiki/Crouzon_syndrome

    Crouzon syndrome is an autosomal dominant genetic disorder known as a branchial arch syndrome. Specifically, this syndrome affects the first branchial (or pharyngeal) arch, which is the precursor of the maxilla and mandible. Because the branchial arches are important developmental features in a growing embryo, disturbances in their development ...

  3. Crouzonodermoskeletal syndrome - Wikipedia

    en.wikipedia.org/wiki/Crouzonodermoskeletal_syndrome

    Crouzonodermoskeletal syndrome is a disorder characterized by the premature joining of certain bones of the skull (craniosynostosis) during development and a skin condition called acanthosis nigricans. Some of the signs and symptoms of Crouzonodermoskeletal syndrome are similar to those seen with Crouzon syndrome.

  4. Apert syndrome - Wikipedia

    en.wikipedia.org/wiki/Apert_syndrome

    Apert syndrome is a form of acrocephalosyndactyly, a congenital disorder characterized by malformations of the skull, face, hands and feet. It is classified as a branchial arch syndrome, affecting the first branchial (or pharyngeal) arch, the precursor of the maxilla and mandible. Disturbances in the development of the branchial arches in fetal ...

  5. Hearing loss with craniofacial syndromes - Wikipedia

    en.wikipedia.org/wiki/Hearing_loss_with...

    Literature has suggested that persons with Crouzon syndrome typically have conductive hearing loss caused by middle ear effusion (or fluid in the middle ear) and perforation to ossicular fixation (ossicles), intratympanic bony masses (tympanic membrane), ossicular anomalies and closure of the oval window. Patients with a sensorineural hearing ...

  6. Turricephaly - Wikipedia

    en.wikipedia.org/wiki/Turricephaly

    Turricephaly is a type of cephalic disorder where the head appears tall with a small length and width. [3][4] It is due to premature closure of the coronal suture plus any other suture, like the lambdoid, [5] or it may be used to describe the premature fusion of all sutures. [2] It should be differentiated from Crouzon syndrome.

  7. Pierre Robin sequence - Wikipedia

    en.wikipedia.org/wiki/Pierre_Robin_sequence

    Pierre Robin sequence [a] (/ p j ɛər r ɔː ˈ b æ̃ /; [3] abbreviated PRS) is a congenital defect observed in humans which is characterized by facial abnormalities.The three main features are micrognathia (abnormally small mandible), which causes glossoptosis (downwardly displaced or retracted tongue), which in turn causes breathing problems due to obstruction of the upper airway.

  8. Octave Crouzon - Wikipedia

    en.wikipedia.org/wiki/Octave_Crouzon

    Octave Crouzon. Louis Édouard Octave Crouzon (1874–1938) was a French neurologist born in Paris. He received his doctorate from the University of Paris, where he studied under Paul Georges Dieulafoy (1839–1911), Joseph Babinski (1857–1932) and Pierre Marie (1853–1940). During his medical career, he was associated with the Hôtel-Dieu ...

  9. Dolichocephaly - Wikipedia

    en.wikipedia.org/wiki/Dolichocephaly

    Dolichocephaly (derived from the Ancient Greek δολιχός 'long' and κεφαλή 'head') is a term used to describe a head that is longer than average relative to its width. In humans, scaphocephaly is a form of dolichocephaly. Dolichocephalic dogs (such as the Lurcher or German Shepherd) have elongated noses. This makes them vulnerable to ...