Rohrback Syndrome

Rohrback Syndrome is a genetic disorder caused by abnormal imprinting of the Chromosomes 15 in the human genome. It is primarly characterized by subtle skull abnormalities, childhood anorexia, dyspolia and severely accelerated aging and excessive facial hair.

Symptoms
Principal features of Rohrback Syndrome (chromosomes 15 have mixed paternal and maternal imprints)


 * Dyspolia
 * Cataholism
 * Anorexia
 * Neonatal	hypertonia
 * Excessive	aging
 * Hypophagia/Aphagia
 * Extreme	underweightness
 * Catatonia
 * Parkinsonisms
 * Hypersexuality
 * Physical	traits
 * Brachycephaly
 * Nystagmus
 * Small		teeth
 * Large		hands and feet
 * Thin	upper-face/small forehead
 * Large	eyes
 * Taller	face
 * Thin	mouth
 * Thin	eyebrows
 * Wide	cheekbones
 * Thin	chin
 * Low	weight
 * Pale	skin
 * Dark	eye sockets
 * Pointed	nose
 * Protrudent	ears


 * Uncontrollable	crying
 * Seemingly	depressed demeanor
 * Ganser	Syndrome