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  2. Trigonocephaly - Wikipedia

    en.wikipedia.org/wiki/Trigonocephaly

    The incidence of metopic synostosis is roughly between 1:700 and 1:15,000 newborns globally (differs per country). [11] [55] Trigonocephaly is seen more in males than females ranging from 2:1 to 6.5:1. [37] [56] [27] [28] Hereditary relations in metopic synostosis have been found of which 5.5% were well defined syndromic. [11]

  3. 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]

  4. Kleeblattschaedel - Wikipedia

    en.wikipedia.org/wiki/Kleeblattschaedel

    Kleeblattschaedel is a rare malformation of the head where there is a protrusion of the skull and broadening of the face. [2] This condition is a severe type of craniosynostosis. [3] The condition can be both isolated or associated with other craniofacial dysostosises. [4] 85% of children with this condition have other anomalies. [5]

  5. 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] thereby changing the growth pattern of the skull. [3]

  6. 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.

  7. 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.

  8. Benign paroxysmal torticollis - Wikipedia

    en.wikipedia.org/wiki/Benign_paroxysmal_torticollis

    The defining characteristic of BPT is a tilting of an infant's head in recurrent episodes, for varying periods of time. [ 1 ] [ 2 ] Furthermore, the child's trunk may bend in the same direction as the head, giving the baby an overall curved shape; this complaint is known as tortipelvis.

  9. Plagiocephaly - Wikipedia

    en.wikipedia.org/wiki/Plagiocephaly

    Plagiocephaly, also known as flat head syndrome, [1] [2] is a condition characterized by an asymmetrical distortion (flattening of one side) of the skull.A mild and widespread form is characterized by a flat spot on the back or one side of the head caused by remaining in a supine position for prolonged periods.