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Anonychia is the failure to form fingernails or toenails. [ 1 ] It is an anomaly which may be the result of a congenital ectodermal defect, ichthyosis , severe infection, severe allergic contact dermatitis , self-inflicted trauma , Raynaud phenomenon , lichen planus , epidermolysis bullosa , or severe exfoliative diseases.
Cooks syndrome is a hereditary disorder which is characterized in the hands by bilateral nail hypoplasia on the thumb, index finger, and middle finger, absence of fingernails on the ring finger and little finger, lengthening of the thumbs, and bulbousness of the fingers.
Onychorrhexis also known as brittle nails, is brittleness with breakage of fingernails or toenails. Paronychia is a bacterial or fungal infection where the nail and skin meet. Koilonychia is when the nail curves upwards (becomes spoon-shaped) due to an iron deficiency. The normal process of change is: brittle nails, straight nails, spoon-shaped ...
Are your fingernails yellow, brown, black, or another color? Doctors explain the different causes of nail discoloration, and what to do in each case. ... Doctors explain the different causes of ...
Nail–patella syndrome is a genetic disorder that results in small, poorly developed nails and kneecaps, but can also affect many other areas of the body, such as the elbows, chest, and hips. The name "nail–patella" can be very misleading because the syndrome often affects many other areas of the body, including even the production of ...
Individuals with this condition typically have the following symptoms: complete absence of both the deciduous and permanent teeth, cone-shaped canines and incisors, generalized dysplasia of the nails, palmoplantar hyperkeratosis, chronic skin dryness, and variable degrees of both hypotrichosis and either hyperhidrosis or hypohidrosis. [1] [2]
Alana Severs had ignored the line on her fingernail for years, covering it up with red nail varnish. Skip to main content. 24/7 Help. For premium support please call: 800-290-4726 ...
Bart syndrome, also known as aplasia cutis congenita type VI, is a rare genetic disorder characterized by the association of congenital localized absence of skin, mucocutaneous blistering and absent and dystrophic nails.