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  2. Trigonocephaly - Wikipedia

    en.wikipedia.org/wiki/Trigonocephaly

    Trigonocephaly is a congenital condition due to premature fusion of the metopic suture (from Ancient Greek metopon 'forehead'), leading to a triangular forehead. The premature merging of the two frontal bones leads to transverse growth restriction and parallel growth expansion.

  3. Carpenter syndrome - Wikipedia

    en.wikipedia.org/wiki/Carpenter_syndrome

    Babies' mobile cranial bones form a cone shape as they pass through the birth canal and soon thereafter return to a normal shape; however, a baby affected by carpenter syndrome maintains a cone shaped head. [citation needed] A baby affected by Carpenter syndrome will also display malformations of the face.

  4. Craniosynostosis - Wikipedia

    en.wikipedia.org/wiki/Craniosynostosis

    The head circumference and the growth curve of the head provide important clues into making a differentiation between craniosynostosis, primary microcephaly and hydrocephalus. [17] This differentiation has an important influence on the further treatment of the child.

  5. Kleeblattschaedel - Wikipedia

    en.wikipedia.org/wiki/Kleeblattschaedel

    The distinctive head shape seen in kleeblattschaedel is caused by the closure of the sagittal, coronal, and lambdoid sutures, with subsequent bulging of the cranial contents leading to a trilobate head shape. [7] The condition is also caused by absence of the coronal and lambdoid sutures. [10] Conditions with kleeblattschaedel include: [11] [12]

  6. 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]

  7. Saethre–Chotzen syndrome - Wikipedia

    en.wikipedia.org/wiki/Saethre–Chotzen_syndrome

    One of the common symptoms of SCS is the development of short (brachydactyly), webbed fingers and broad toes . These characteristics do not cause any problems to the function of the hands or feet, and thus, no medical procedure is required to fix the abnormalities, unless the patient requests it.

  8. 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.

  9. File:Birth to 36 months boys head circumference clinical ...

    en.wikipedia.org/wiki/File:Birth_to_36_months...

    Short title: Birth to 36 months: Boys, Head circumberence-for-age and Weight-for-length percentiles: Image title: CDC Growth Charts: United States: Author