Question

It is a rare genetic disease
in which the child shows
premature ageing, the loss
of body fat, loss of hair,
stiffness in the joints and
hip dislocation.​

Answer 1

Answer:

Progeria, or Hutchinson-Gilford progeria syndrome (HGPS), is a rare, fatal, genetic condition of childhood with striking features resembling premature aging. Children with progeria usually have a normal appearance in early infancy

Explanation:

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