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: Frontotemporal dementia Detailed Information
Frontotemporal dementia (frontotemporal lobar degeneration) is an umbrella phrase for a various group of infrequent disorders. Frontotemporal Dementia (FTD) is an umbrella term for a group of rare disorders that mainly affect the frontal and temporal lobes of the brain – the areas commonly associated with personality and behaviour....
Frontotemporal dementia (frontotemporal lobar degeneration) is an umbrella phrase for a various group of infrequent disorders. Frontotemporal Dementia (FTD) is an umbrella term for a group of rare disorders that mainly affect the frontal and temporal lobes of the brain – the areas commonly associated with personality and behaviour....
: Friedreich Ataxia Detailed Information
Friedreich's Ataxia is a gradually progressive disorder of the nervous system and muscles. This condition is caused by degeneration of nerve tissue in the spinal cord and of nerves that expand to peripheral areas such as the arms and legs....
Friedreich's Ataxia is a gradually progressive disorder of the nervous system and muscles. This condition is caused by degeneration of nerve tissue in the spinal cord and of nerves that expand to peripheral areas such as the arms and legs....
: Frey's syndrome Detailed Information
Frey's syndrome also known as Baillarger’s syndrome, Dupuy’s syndrome, Auriculotemporal syndrome or Frey-Baillarger syndrome. Frey's Syndrome is a rare neurological disorder that results from injury or surgery near the parotid glands (which manufacture saliva), damaging the facial nerve. ...
Frey's syndrome also known as Baillarger’s syndrome, Dupuy’s syndrome, Auriculotemporal syndrome or Frey-Baillarger syndrome. Frey's Syndrome is a rare neurological disorder that results from injury or surgery near the parotid glands (which manufacture saliva), damaging the facial nerve. ...
: Freiberg's disease Detailed Information
Freiberg's disease an osteochondrosis affecting the toes: the articular surfaces of the second or third metatarsal heads collapse. It is commonest in girls aged 12-15 years. It causes pain on weight bearing and restricts physical activity. ...
Freiberg's disease an osteochondrosis affecting the toes: the articular surfaces of the second or third metatarsal heads collapse. It is commonest in girls aged 12-15 years. It causes pain on weight bearing and restricts physical activity. ...
: Freeman-Sheldon syndrome Detailed Information
Freeman-Sheldon syndrome is a very rare genetic condition. Freeman-sheldon syndrome is characterized by multiple contractures (i.e., restricted faction around two or more body areas) at birth (congenital), abnormalities of the head and face (craniofacial) area, defects of the hands and feet, and skeletal malformations. ...
Freeman-Sheldon syndrome is a very rare genetic condition. Freeman-sheldon syndrome is characterized by multiple contractures (i.e., restricted faction around two or more body areas) at birth (congenital), abnormalities of the head and face (craniofacial) area, defects of the hands and feet, and skeletal malformations. ...
: Fraser syndrome Detailed Information
Fraser syndrome is a uncommon genetic syndrome with abnormalities of the head, lungs, kidneys, and limbs. Fraser syndrome is also referred to as crytophthalmos with extra malformations because over 90% of the people born with this syndrome have hidden (crypto-) eyes (ophthalmos)....
Fraser syndrome is a uncommon genetic syndrome with abnormalities of the head, lungs, kidneys, and limbs. Fraser syndrome is also referred to as crytophthalmos with extra malformations because over 90% of the people born with this syndrome have hidden (crypto-) eyes (ophthalmos)....
: Fragile X syndrome Detailed Information
Fragile X is a family of genetic conditions. Fragile X syndrome also known Martin-Bell syndrome. It is caused by an abnormality in a single gene. Fragile X syndrome caused by mutation of the FMR1 gene on the X chromosome....
Fragile X is a family of genetic conditions. Fragile X syndrome also known Martin-Bell syndrome. It is caused by an abnormality in a single gene. Fragile X syndrome caused by mutation of the FMR1 gene on the X chromosome....
: Fox-Fordyce disease Detailed Information
Fox-Fordyce disease is an rarely happing chronic pruritic papular eruption that place to areas where apocrine glands are create. This condition is also referred to as ‘apocrine duct occlusion’ and ‘sweat retention disease’. ...
Fox-Fordyce disease is an rarely happing chronic pruritic papular eruption that place to areas where apocrine glands are create. This condition is also referred to as ‘apocrine duct occlusion’ and ‘sweat retention disease’. ...
: Follicular lymphoma Detailed Information
Follicular lymphoma is the most common of the indolent non-Hodgkin's lymphomas. Non-Hodgkin lymphoma is a heterogeneous group of malignancies of lymphocyte origin that usually arise or are present in lymphoid tissues....
Follicular lymphoma is the most common of the indolent non-Hodgkin's lymphomas. Non-Hodgkin lymphoma is a heterogeneous group of malignancies of lymphocyte origin that usually arise or are present in lymphoid tissues....
: Fissured tongue Detailed Information
Fissured tongue, also called scrotal tongue. Fissured tongue is a benign condition characterized by deep grooves (fissures) in the dorsum of the tongue....
Fissured tongue, also called scrotal tongue. Fissured tongue is a benign condition characterized by deep grooves (fissures) in the dorsum of the tongue....
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