Sponsored Link
1- Cutaneous Horns
Cutaneous horns, also known by the Latin name cornu cutaneum, are unusual keratinous skin tumors with the appearance of horns, or sometimes of wood or coral.
2- Neurofibromatosis
Neurofibromatosis (NF) refers to a number of inherited conditions that are clinically and genetically distinct and carry a high risk of tumor formation, particularly in the brain. Neurofibromatosis is an autosomal dominant disorder, which means only one copy of the affected gene is needed for the disorder to develop.
3-Noma
Noma (also referred to as cancrum oris, fusospirochetal gangrene, necrotizing ulcerative stomatitis, stomatitis gangrenosa) is a rapidly progressive, polymicrobial, often gangrenous infection of the mouth or genitals.
4- Polyostotic Fibrous Dysplasia
People with McCune-Albright syndrome develop areas of abnormal scar-like (fibrous) tissue in their bones, a condition called polyostotic fibrous dysplasia.
5-Progeria
Progeria is an extremely rare genetic disorder wherein symptoms resembling aspects of aging are manifested at a very early age.
6-Epidermodysplasia Verruciformis
This colloquially known as tree man illness is an extremely rare autosomal recessive genetic hereditary skin disorder associated with a high risk of carcinoma of the skin. It is characterized by abnormal susceptibility to human papillomaviruses (HPVs) of the skin
7-Polymelia
Polymelia is a birth defect involving limbs (a type of dysmelia), in which the affected individual has more than the usual number of limbs. In humans and most land-dwelling animals, this means having five or more limbs. The extra limb is most commonly shrunken and/or deformed.
8-Diprosopus
Diprosopus is an extremely rare congenital disorder whereby parts (accessories) or all of the face are duplicated on the head.
9-Haemangioma
A hemangioma is a benign and usually self-involuting tumor (swelling or growth) of the endothelial cells that line blood vessels, and is characterised by increased number of normal or abnormal vessels filled with blood.
10-Hidrocefalia Hidrocefalia is a medical condition in which there is anabnormal accumulation of cerebrospinal fluid (CSF) in the ventricles of the brain. This causes increased intracranial pressure inside the skull and may cause progressive enlargement of the head if it occurs in childhood, convulsion, tunnel vision, and mental disability.
Follow OMOPedia on Twitter!
Like OMOPEDIA on Facebook!
Cutaneous horns, also known by the Latin name cornu cutaneum, are unusual keratinous skin tumors with the appearance of horns, or sometimes of wood or coral.
2- Neurofibromatosis
Neurofibromatosis (NF) refers to a number of inherited conditions that are clinically and genetically distinct and carry a high risk of tumor formation, particularly in the brain. Neurofibromatosis is an autosomal dominant disorder, which means only one copy of the affected gene is needed for the disorder to develop.
Noma (also referred to as cancrum oris, fusospirochetal gangrene, necrotizing ulcerative stomatitis, stomatitis gangrenosa) is a rapidly progressive, polymicrobial, often gangrenous infection of the mouth or genitals.
4- Polyostotic Fibrous Dysplasia
People with McCune-Albright syndrome develop areas of abnormal scar-like (fibrous) tissue in their bones, a condition called polyostotic fibrous dysplasia.
5-Progeria
Progeria is an extremely rare genetic disorder wherein symptoms resembling aspects of aging are manifested at a very early age.
6-Epidermodysplasia Verruciformis
This colloquially known as tree man illness is an extremely rare autosomal recessive genetic hereditary skin disorder associated with a high risk of carcinoma of the skin. It is characterized by abnormal susceptibility to human papillomaviruses (HPVs) of the skin
7-Polymelia
Polymelia is a birth defect involving limbs (a type of dysmelia), in which the affected individual has more than the usual number of limbs. In humans and most land-dwelling animals, this means having five or more limbs. The extra limb is most commonly shrunken and/or deformed.
8-Diprosopus
Diprosopus is an extremely rare congenital disorder whereby parts (accessories) or all of the face are duplicated on the head.
9-Haemangioma
A hemangioma is a benign and usually self-involuting tumor (swelling or growth) of the endothelial cells that line blood vessels, and is characterised by increased number of normal or abnormal vessels filled with blood.
10-Hidrocefalia Hidrocefalia is a medical condition in which there is anabnormal accumulation of cerebrospinal fluid (CSF) in the ventricles of the brain. This causes increased intracranial pressure inside the skull and may cause progressive enlargement of the head if it occurs in childhood, convulsion, tunnel vision, and mental disability.
Like OMOPEDIA on Facebook!
Post a Comment Blogger Facebook