1. World problems
  2. Dwarfism

Dwarfism

  • Microsomia
  • Fröhlich's syndrome
  • Simmonds' disease

Nature

Dwarfism, or restricted growth, is usually a genetic condition resulting in short stature of a child with parents of normal height. It may also be developed as a result of organic disease or determined by environmental factors in the case of a genetically susceptible individual. Only where dwarf height occurs in defined racial populations can the condition be considered hereditary.

Microsomia has three forms: in the first one there is only a deficiency in stature; in the second one additional serious hypogenesis of the skeleton except for a large skull is present; and in the third one includes a combination of infantilism and premature senility. Racial dwarfism occurs in some groups whose physiological bodily functions are otherwise quite normal. Sub-normal height creates a multitude of special problems for such individuals in relating to others and in using facilities designed for those of average height.

Incidence

The normal height of adult men has been arbitrarily set at 150 cm, and on this basis dwarf populations exist in Central Africa, the Andaman Islands, Philippines, and New Guinea. The pygmies of Central Africa have heights down to 120 cm.

Broader

Narrower

Renal dwarfism
Yet to rate

Aggravates

Aggravated by

Related

Value

Syndrome
Yet to rate
Disease
Yet to rate

Reference

Web link

SDG

Sustainable Development Goal #3: Good Health and Well-being

Metadata

Database
World problems
Type
(E) Emanations of other problems
Subject
  • Medicine » Malformations
  • Medicine » Pathology
  • Content quality
    Presentable
     Presentable
    Language
    English
    Last update
    Oct 4, 2020