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  2. Craniosynostosis - Wikipedia

    en.wikipedia.org/wiki/Craniosynostosis

    Children born with craniosynostosis have a distinct phenotype, i.e., appearance—observable traits caused by the expression of a condition's genes. The features of craniosynostosis' particular phenotype are determined by which suture is closed. [7] The fusion of this suture causes a certain change in the shape of the skull; a deformity of the ...

  3. Craniosynostosis with anomalies of the cranial base and digits

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

    The big toes may also be missing or improperly positioned. Additionally, the bones in the skull close too early in development (craniosynostosis), and bones at the skull base grow incorrectly. [1] Woon et al. first reported the condition in 1980 in a pair of male twins of Mexican American and Sioux Indian ancestry with no chromosomal ...

  4. 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.

  5. 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 ...

  6. Pfeiffer syndrome - Wikipedia

    en.wikipedia.org/wiki/Pfeiffer_syndrome

    Pfeiffer syndrome is a rare genetic disorder, characterized by the premature fusion of certain bones of the skull (craniosynostosis), which affects the shape of the head and face. The syndrome includes abnormalities of the hands and feet, such as wide and deviated thumbs and big toes.

  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. 10 weird things that can kill you almost instantly - AOL

    www.aol.com/news/2016-03-13-10-weird-things-that...

    Most victims fell to their deaths, while others drowned, got struck by trains, were shot, or were involved in a fatal car crash. See photos of people taking questionable selfies: Number 2.

  9. Kleeblattschaedel - Wikipedia

    en.wikipedia.org/wiki/Kleeblattschaedel

    Kleeblattschaedel (Kleeblattschädel) is German for "cloverleaf skull". [6] The disorder was named Kleeblattschaedel syndrome in 1958. [7] The German word is sometimes used in medical English, where it is often regarded as more or less naturalized, thus appearing in any combination of capitalized or not, with umlaut diacritic or not, and italicized or not.