Progeria, also known as Hutchinson-Gilford syndrome, is an extremely rare, progressive genetic disorder that causes children to age rapidly, starting in their first two years of life. Children with progeria generally appear normal at birth....See More

Hutchinson-Gilford Progeria Syndrome (HGPS) since 1886. HGPS is an extremely rare genetic disorder in which the symptoms resemble aspects of ageing at a very early age. The condition affects one in eight million live births and those bor...See More

A patient 22/m burning, ulcerated penis. According to symptoms I selected merc. Sol 200, stysphygeria 200.all complaints...See More

Acrogeria a rare condition. Acrogeria condition is characterized by nonprogressive form of skin atrophy mainly in the ...See More

A female patient Of six years and eleven months old was brought to clinic. she was deleiverd normally with all parameter...See More

Diagnosis..? Is it prigeria?

a very interesting case of progeria. lets discuss all the possible outcomes and reasons for the same