The following Conditions are related to Short neck

Select a specific condition below to view its details.

  • Harrington syndrome

    Chromosome 10, monosomy 10p is a rare chromosomal disorder in which the end (distal) portion of the short arm (p) of chromosome 10 is missing (deleted or monosomic). The range and severity of symptoms and findings may be variable, depending upon the exact size or location of the deletion on chromosome 10p. However, associated features often include severe intellectual disability; growth delays after birth (postnatal growth retardation); distin  Read More

  • Mucopolysaccharidosis iv

    Morquio syndrome (mucopolysaccharidosis type IV; MPS IV) is a mucopolysaccharide storage disease that exists in two forms (Morquio syndromes A and B) and occurs because of a deficiency of the enzymes N-acetyl-galactosamine-6-sulfatase and beta-galactosidase, respectively. A deficiency of either enzyme leads to the accumulation of mucopolysaccharides in the body, abnormal skeletal development, and additional symptoms. In most cases, individuals  Read More

  • Trigonocephaly syndrome

    The complex condition known as trigonocephaly syndrome (OTCS) is associated with a wide variety of clinical characteristics and anomalies. This preliminary diagnosis may be given to children, who may later be found to have a particular genetic disorder. Affected children are born with trigonocephaly, a malformation characterized by a triangular-shaped head, a narrow pointed forehead, a flat, broad nasal bridge wit  Read More