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Autosomal dominant aplasia cutis in three generations and one case with preaxial polydactyly in the last generation.
- Source :
-
Genetic counseling (Geneva, Switzerland) [Genet Couns] 2011; Vol. 22 (1), pp. 55-61. - Publication Year :
- 2011
-
Abstract
- Aplasia Cutis Congenita (ACC), characterized by the focal absence of the skin and skin adnexia resulting from a developmental failure, may occur as part of Adams-Oliver Syndrome (AOS) which can be defined as a congenital inherited disorder, consisting of terminal transverse limb defects and vascular anomalies in addition to ACC. Coexistence of isolated preaxial polydactyly without terminal extremity defect and ACC is extremely rare. Furthermore, ACC and preaxial polydactyly has not been reported previously. Here we report a three-generation family with autosomal dominant aplasia cutis congenita and preaxial polydactyly in the last generation and discuss whether it is a coincidence or not.
- Subjects :
- Ectodermal Dysplasia diagnosis
Ectodermal Dysplasia pathology
Female
Humans
Infant
Infant, Newborn
Limb Deformities, Congenital diagnosis
Limb Deformities, Congenital genetics
Limb Deformities, Congenital pathology
Male
Pedigree
Polydactyly diagnosis
Polydactyly genetics
Scalp pathology
Scalp Dermatoses congenital
Scalp Dermatoses diagnosis
Scalp Dermatoses genetics
Scalp Dermatoses pathology
Thumb abnormalities
Chromosome Aberrations
Ectodermal Dysplasia genetics
Genes, Dominant genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1015-8146
- Volume :
- 22
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Genetic counseling (Geneva, Switzerland)
- Publication Type :
- Academic Journal
- Accession number :
- 21614989