GENODERMATOSES

Hypomelanosis of Ito
Gardner syndrome
Pseudoxanthoma elasticum
Ehler Danlos syndrome
Ataxia telangiectasia
Cowden syndrome
Peutz Jegher syndrome
Howel Evans syndrome
POROKERATOSIS
Basal cell nevus syndrome
Proteus syndrome
Collagenoma
Cockayne syndrome
Cutis Laxa
KERATOSIS PILARIS
DYSKERATOSIS CONGENITA
DYSKERATOSIS CONGENITA
BLOOM SYNDROME
Genodermatoses (genetic diseases)
Hereditary disease
Congenital disease
Chromosome
Autosomal inheritance
Autosomal dominant (AD)
Autosomal recessive (AR)
CLASSIFICATION OF SKIN DISEASES ACCORDING TO THE TYPE OF GENE PRODUCT OR TARGETED Ag INVOLVED
NEUROFIBROMATOSIS (VON RECK INGHAUSEN DISEASE)
DARIER DISEASE (KERATOSIS FOLLICULARIS)
ACROKERATOSIS VERRUCIFORMIS (HOPF)
TUBEROUS SCLEROSIS (EPILOA)
PREMATURE AGING SYNDROMES
CONNECTIVE TISSUE NEVI
MRFAN SYNDROME
GENODERMATOSES WITH POIKILODERMA OR TELANGIECTASIA
GENODERMATOSES WITH CELLULAR HYPERSENSITIVITY
PALMOPLANTAR KERATODERMAS
CONGENITAL ECTODERMAL DEFECTS (DYSPLASIAS)
FOCAL DERMAL HYPOPLASIA SYNDROME (GOLTZ SYNDROME)
APLASIA CUTIS CONGENITA
PACHYDERMOPERIOSTOSIS
INCONTINENTIA PIGMENTI
BLASCHKO’S LINES
ICHTHYOSES
PANGERIA (WERNER SYNDROME) (ADULT PROGERIA)
PROGERIA (HUTCHINSON GILFORD SYNDROME)
ACROGERIA (GOTTRON SYNDROME)
SHAGREEN PATCH
HUNTER SYNDROME
X linked dominant inheritance (XLD)
X linked recessive inheritance (XLR)
POIKILODERMA CONGENITALE (ROTHMUND THOMSON SYNDROME)
CONGENITAL TELANGIECTATIC ERYTHEMA (BLOOM SYNDROME)
AKA Louis Barr Syndrome
MOON’S CHILDREN DISEASE
Fanconi anemia
Hereditary keratodermas
Unna Thost syndrome
Epidermolytic PPK
Mutilating PPK
Punctate PPK
Progressive PPK
Mal de meleda syndrome
Papillon Lefevre syndrome
Keratoderma with other syndromes
PRP.
Acrokeratoelastoidosis of COSTA
Pachyonychia congenita
Nevoid BCC. Syndrome
Acquired keratodermas
Keratoderma climactericum
Reiter disease (Keratoderma blenorrhagica)
Paraneoplastic keratoderma
Porokeratosis of Mibelli
Disseminated Superficial Actinic Porokeratosis
Linear Porokeratosis
Porokeratosis Palmaris Plantaris et Disseminata
Punctate porokeratosis
GENERALIZED BASELOID FOLLICULAR HAMARTOMA SYNDROME
PRIMARY ICHTHYOSES
Ichthyosis vulgaris
X linked recessive ichthyosis
Ichthyosis bullosa of Siemens
Autosomal recessive ichthyoses (COLLODION BABY)
Non bullous congenital ichthyosiform erythroderma
Lamellar ichthyosis (non erythrodermic)
ICHTHYOSIFORM SYNDROMES
KID SYNDROME
NETHERTON SYNDROME
CHILD SYNDROME
SJOGREN LARSSONE SYNDROME
Ichthyosis Follicularis (IFAP Syndrome)
REFSUM DISEASE/SYNDROME
DORFMAN CHANARIN SYNDROME (NATURAL LIPID STORAGE DISEASE)
RUD SYNDROME
CONRADI SYNDROME
Conradi Hunermann Syndrome
IBID SYNDROME (TAY’S SYNDROME)
ACQUIRED ICHTHYOSIS
PITYRIASIS ROTUNDA
RELATED DISORDERS OF CORNIFICATION
Erythrokeratoderma variabilis
Progressive Symmetric Erythrokeratodermia
Ichthyosis linearis circumflexa
Harlequin ichthyosis
Klinefelter’s Syndrome
Noonan’s Syndrome
Cardio Facio Cutaneous Synd.
Epidermolytic Hyperkeratosis(Bullous Congenital Ichthyosiform Erythroderma)