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Aplasia cutis congenita | About the Disease | GARD
Aplasia cutis congenita is a condition in which there is congenital (present from birth) absence of skin, with or without the absence of underlying structures such as bone. It most commonly affects the scalp, but any location of the body can be affected.
Aplasia cutis congenita - UpToDate
2023年7月21日 · Aplasia cutis congenita (ACC) is a rare, heterogeneous group of congenital disorders characterized by focal or widespread absence of the skin [1,2]. ACC can occur anywhere on the body, but most cases occur on the scalp.
Aplasia Cutis Congenita - StatPearls - NCBI Bookshelf
2023年7月31日 · Aplasia cutis congenita (ACC) is a rare congenital skin defect characterized by a focal or extensive absence of the epidermis, dermis, and occasionally subcutaneous tissue. The exact etiology of ACC is not well understood; however, it is …
Aplasia cutis congenita - DermNet
What is aplasia cutis congenita? Aplasia cutis congenita describes the congenital absence of skin. The commonest form presents as a scalp defect at birth. Aplasia cutis is also a component of a number of genetic syndromes.
Aplasia Cutis Congenita - Symptoms, Causes, Treatment | NORD
2007年8月9日 · Aplasia Cutis Congenita is a rare disorder with a complicated pattern of inheritance. Babies are born with the absence of certain layer (s) of skin, most often on the scalp, but also on the trunk, and/or arms and legs. The affected area is typically covered with a thin, transparent membrane.
Aplasia Cutis Congenita | NeoReviews | American Academy of ...
2012年5月1日 · Aplasia cutis congenita (ACC) is a rare disorder that is estimated to affect approximately three newborns in every 10,000 live births. It is usually detected at birth and most commonly affects the scalp as a solitary lesion.
Aplasia cutis congenita - Wikipedia
Aplasia cutis congenita is a rare disorder characterized by congenital absence of skin. Ilona J. Frieden classified ACC in 1986 into 9 groups on the basis of location of the lesions and associated congenital anomalies. [2] The scalp is the most commonly involved area with lesser involvement of trunk and extremities.
Aplasia Cutis Congenita: Background, Pathophysiology, Etiology
2020年6月16日 · First reported by Cordon in 1767, aplasia cutis congenita manifests as a solitary defect on the scalp in 70% of cases, but it may sometimes occur as multiple lesions. Although most...
Aplasia Cutis Congenita: Symptoms, Causes & Treatment
Aplasia Cutis Congenita (ACC) is a rare congenital disorder characterized by the absence of skin in localized or widespread areas of the body. This condition primarily manifests at birth, and though it may occur anywhere on the body, it most frequently affects the scalp.
Orphanet: Aplasia cutis congenita
A rare skin disorder characterized by localized absence of skin that is usually located on the scalp but can occur anywhere on the body including the face, trunk and extremities. Aplasia cutis congenita (ACC) may occasionally be associated with other anomalies.