Aplasia cutis congenita
Encyclopedia
Aplasia cutis congenita is the most common congenital cicatricial alopecia
, and is a congenital focal absence of epidermis with or without evidence of other layers of the skin.
It can be associated with Johanson-Blizzard syndrome
, Adams-Oliver syndrome
, trisomy 13, and Wolf-Hirschhorn syndrome
.
It is also seen with exposure to Methimazole
in utero. This dermatological manifestation has been linked to Peptidase D haploinsufficiency and a deletion in Chromosome 19.
a form of aplasia cutis is also seen in patau syndrome (trisomy 13)
en.wikipedia.org/wiki/patau_syndrome
Cicatricial alopecia
The term cicatricial alopecia refers to a diverse group of rare disorders that destroy the hair follicle, replace it with scar tissue, and cause permanent hair loss. A variety of distributions are possible. In some cases, hair loss is gradual, without symptoms, and is unnoticed for long periods...
, and is a congenital focal absence of epidermis with or without evidence of other layers of the skin.
It can be associated with Johanson-Blizzard syndrome
Johanson-Blizzard syndrome
Johanson–Blizzard syndrome is a rare, sometimes fatal autosomal recessive multisystem congenital disorder featuring abnormal development of the pancreas, nose and scalp, with mental retardation, hearing loss and growth failure...
, Adams-Oliver syndrome
Adams-Oliver syndrome
Adams–Oliver syndrome is a rare congenital disorder characterized by defects of the scalp and cranium , transverse defects of the limbs, and mottling of the skin.- Characteristics :...
, trisomy 13, and Wolf-Hirschhorn syndrome
Wolf-Hirschhorn syndrome
Wolf–Hirschhorn syndrome , also known as chromosome deletion 4p syndrome, Pitt-Rogers-Danks syndrome or Pitt syndrome, was first described in 1961 by Americans Herbert L...
.
It is also seen with exposure to Methimazole
Methimazole
Methimazole is an antithyroid drug, and part of the thioamide group.-Indications:...
in utero. This dermatological manifestation has been linked to Peptidase D haploinsufficiency and a deletion in Chromosome 19.
See also
a form of aplasia cutis is also seen in patau syndrome (trisomy 13)
en.wikipedia.org/wiki/patau_syndrome