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  2. Craniosynostosis - Wikipedia

    en.wikipedia.org/wiki/Craniosynostosis

    Craniosynostosis is a condition in which one or more of the fibrous sutures in a young infant's skull prematurely fuses by turning into bone (ossification), [2] ...

  3. List of conditions with craniosynostosis - Wikipedia

    en.wikipedia.org/wiki/List_of_conditions_with...

    Craniosynostosis, a condition in which the sutures of the head (joints between the bones of the skull) prematurely fuse and subsequently alter the shape of the head, is seen in multiple conditions, as listed below. The level of involvement varies by condition and can range from minor, single-suture craniosynostosis to major, multisutural ...

  4. Synostosis - Wikipedia

    en.wikipedia.org/wiki/Synostosis

    craniosynostosis – an abnormal fusion of two or more cranial bones; radioulnar synostosis – the abnormal fusion of the radius and ulna bones of the forearm; tarsal coalition – a failure to separately form all seven bones of the tarsus (the hind part of the foot) resulting in an amalgamation of two bones; and

  5. Craniosynostosis with anomalies of the cranial base and digits

    en.wikipedia.org/wiki/Craniosynostosis_with...

    Craniosynostosis with anomalies of the cranial base and digits is a syndrome characterized by atypical development in a fetus's limbs and skull. People with this condition are often missing the middle parts of the second and fifth fingers, as well as their thumbs, though the thumbs may be improperly positioned.

  6. Muenke syndrome - Wikipedia

    en.wikipedia.org/wiki/Muenke_syndrome

    Muenke syndrome, also known as FGFR3-related craniosynostosis, [1] is a human specific condition characterized by the premature closure of certain bones of the skull during development, which affects the shape of the head and face. First described by Maximilian Muenke, the syndrome occurs in about 1 in 30,000 newborns.

  7. Craniosynostosis and dental anomalies - Wikipedia

    en.wikipedia.org/wiki/Craniosynostosis_and...

    Craniosynostosis and dental anomalies (CRSDA, also known as Kreiborg-Pakistani syndrome) is an autosomal recessive syndrome characterized by craniosynostosis, maxillary hypoplasia, and dental anomalies. Dental anomalies seen in this condition include malocclusion, delayed and ectopic tooth eruption, and/or supernumerary teeth.

  8. Baller–Gerold syndrome - Wikipedia

    en.wikipedia.org/wiki/Baller–Gerold_syndrome

    Craniosynostosis involves the pre-mature fusion of bones in the skull. [1] The coronal craniosynostosis that is commonly seen in patients with BGS results in the fusion of the skull along the coronal suture . [ 5 ]

  9. Scaphocephaly - Wikipedia

    en.wikipedia.org/wiki/Scaphocephaly

    Scaphocephaly or sagittal craniosynostosis is a type of cephalic disorder which occurs when there is a premature fusion of the sagittal suture. Premature closure results in limited lateral expansion of the skull , resulting in a characteristic long, narrow head. [ 1 ]