Aplasia cutis congenita (ACC) is a rare genetic disease that causes missing skin in newborns. In some cases of aplasia cutis congenita, underlying structures beneath the skin are also absent.

Aplasia cutis congenita, first described by M. Cordon in 1767, manifests as a single defect on the scalp in 70% of cases, but it can also manifest as numerous lesions.

Aplasia Cutis Congenita (ACC): A congenital absence of skin, typically observed as a focal or extensive defect at birth, most commonly on the scalp.

Aplasia cutis congenita is a rare condition that causes newborns to have skin missing from parts of their body. In some cases, the underlying structures beneath the skin, such as bone, may also ...

Did you know that certain medications can cause symptom of 'Aplasia cutis congenita'. Find these drugs listed on the page and be warned of similar symptoms as possible side-effects.

Aplasia Cutis Congenita (ACC) was first described in two sisters with skin defects of the lower extremities by Cordon in 1767. 1 In 1986, Frieden proposed a classification system for ACC with nine ...

Cite this: Familial Epidermolysis Bullosa With Aplasia Cutis Congenita: Bart's Syndrome? - Medscape - Sep 01, 2003. References. Authors and Disclosures. Authors and Disclosures.

Researchers have revealed the mechanisms behind mutations that cause a congenital condition called aplasia cutis congenita, in which babies are born without skin along the midline of the scalp The ...

Doctors at Methodist Hospital in San Antonio initially diagnosed the baby with aplasia cutis, a rare skin condition in which someone is born without skin, reported the San Antonio Express-News ...

The differential diagnosis of TTA includes AA, trichotillomania, traction alopecia, or aplasia cutis congenita. 6 It is not uncommon for TTA to be initially misdiagnosed as AA.

CASE #2: Aplasia cutis group 1. Aplasia cutis (AC) is a not uncommon condition that manifests with scarring and is related to a lack of skin and skin structures at birth.