Actinic keratosis usually disappears on its own; however, some lesions are difficult to diagnose whether they are normal or they can shift into cancerous lesions.Treatment-In case of Actinic keratosis, it can be difficult to distinguish between noncancerous spots and cancerous ones. So it's best to get evaluated by a doctor.When you have severe actinic keratosis, the doctor may prescribe you a  Read More

Atopic dermatitis facts Atopic dermatitis is a type of eczema. The disease may be inherited and genetically determined. The patient's skin may be "super sensitive" to many irritants. Dry, scaly patches develop in a characteristic distribution. Itching varies but may be intense and scratching hard to resist. Scratching can cause skin thickening and darkening and lead to further co  Read More

A genetic skin condition called hallopeau-siemens disease or dystrophic epidermolysis bullosa causes blisters to grow. One of the more severe types is the Hallopeau-Siemens syndrome type.Due to the defect's location in the dermis at the dermo-epidermal junction, even little skin trauma results in profuse blister production that always heals with scars.Anchoring fibrils are either absent or inadequate due t  Read More

The symptoms of AEC syndrome are highly variable, even among members of the same family. In addition, the small number of identified cases, the lack of large clinical studies, and the possibility of other genes or factors influencing the disorder prevent physicians from developing a completely accurate picture of associated symptoms and prognosis. Affected individuals or their parents should talk to their physician and medical team about their  Read More

Dead skin cells build up in thick, dry scales on the surface of your skin as a result of the genetic skin condition ichthyosis vulgaris.Ichthyosis vulgaris, also known as fish scale disease or fish skin disease, can cause scales to develop from birth, but this is typically when they first do.Because they are frequently mistaken for cases of severely dry skin, modest occurrences of ichthyosis vulgaris can g  Read More

Ichthyosis Vulgaris is caused by an inherited genetic flaw, a mutation that affects a large protein called filaggrin.The faulty gene is inherited from one's parents and may be caused by one or more mutations in the profillagrin gene that occur early in fetal development.It is autosomal dominant, which means that all that is required for the condition is a single faulty copy of the gene that codes for f  Read More

A chronic inflammatory disorder that affects the skin and mucosal membranes is Lichen Annularis.Inflammation (swelling and irritation) on the skin or within the mouth is a common symptom of lichen planus.Your skin develops an itchy rash as a result of Lichen Annularis.Your mouth may become painful or burn.An unidentified protein in the skin and mucosal keratinocytes is the target of infla  Read More

Non-scarring epidermolysis bullosa is a disease that results from mutations in KRT5 or KRT14 gene. These genes provide instructions for making a protein called keratin 5 and 14. There are two major types, and seventeen minor subtypes for this disease, all of which have common effects and symptoms.Among these, the four major subtypes of EBS are here:EBS-loc- in this, blisters are rarely present at birth and ma  Read More

Congenital scalp defects include various conditions of the newborn where there is an absence of skin and sometimes underlying structures of the scalp. These areas on the scalp are of varying sizes and are often hairless.These are most known as Aplasia Cutis Congenita (ACC) and previously called Congenital Ulcer or Streeters spots.Line of treatment generally depends upon the size, width, depth, and locat  Read More

Scalp psoriasis (psoriasis of the scalp) is a disorder that leads to an itchy, raised, reddish, and scaly scalp. It may be present in the form of small watches or cover the entire forehead. Moreover, scalp psoriasis can spread from the scalp to the forehead or back of the neck. It can also result in hair loss. The doctor states that this condition is connected to the immune system. However, it is curable through solutions, lot  Read More

Vitiligo has no known cure. The purpose of medical therapy is to achieve a consistent skin tone by restoring colour (repigmentation) or removing the remaining colour (depigmentation).SurgerySkin grafts obtained from the patient: Skin is taken from one portion of the patient and utilised to cover another. Scarring, infection, and inability to repigment are all possible problems. it can also be called mic  Read More

Vitiligo Capitis is a condition that results in patchy loss of skin pigment. With time, the discoloured spots typically enlarge. Any portion of the body's skin might be impacted by the illness. The tongue and hair can both be impacted by it.Treatment or Cure available for the Vitiligo Capitis conditionThe type of treatment you receive will depend on your age, the location and amount of skin affected  Read More

The symptoms of AEC syndrome are highly variable, even among members of the same family. In addition, the small number of identified cases, the lack of large clinical studies, and the possibility of other genes or factors influencing the disorder prevent physicians from developing a completely accurate picture of associated symptoms and prognosis. Affected individuals or their parents should talk to their physician and medical team about their  Read More

White Darier disease is also named as Keratosis Follicularis.It is a very rare skin disorder and is genetic.It is characterized by lesions on the skin that have thickened, rough bumps i.e., papules that appear greasy, yellow or skin color or brown crust.These lesions may spread and grow over time. This may vary from person to person. This mostly affects scalp, forehead, upper arms, chest, back, kn  Read More