Talk:Integumentary System - Abnormalities

ICD 10 - Other congenital malformations (Q80-Q89)

Links: Integumentary Abnormalities

Q80 Congenital ichthyosis

Excl.: Refsum's disease (G60.1)

• Q80.0 Ichthyosis vulgaris
• Q80.1 X-linked ichthyosis
• Q80.2 Lamellar ichthyosis Collodion baby
• Q80.3 Congenital bullous ichthyosiform erythroderma
• Q80.4 Harlequin fetus
• Q80.8 Other congenital ichthyosis
• Q80.9 Congenital ichthyosis, unspecified

Q81 Epidermolysis bullosa

• Q81.0 Epidermolysis bullosa simplex Excl.: Cockayne's syndrome (Q87.1)
• Q81.1 Epidermolysis bullosa letalis Herlitz' syndrome
• Q81.2 Epidermolysis bullosa dystrophica
• Q81.8 Other epidermolysis bullosa
• Q81.9 Epidermolysis bullosa, unspecified
• Q82 Other congenital malformations of skin Excl.: acrodermatitis enteropathica (E83.2) congenital erythropoietic porphyria (E80.0) pilonidal cyst or sinus (L05.-) Sturge-Weber(-Dimitri) syndrome (Q85.8)
• Q82.0 Hereditary lymphoedema
• Q82.1 Xeroderma pigmentosum
• Q82.2 Mastocytosis Urticaria pigmentosa Excl.: malignant mastocytosis (C96.2)
• Q82.3 Incontinentia pigmenti
• Q82.4 Ectodermal dysplasia (anhidrotic) Excl.: Ellis-van Creveld syndrome (Q77.6)
• Q82.5 Congenital non-neoplastic naevus Birthmark NOS Naevus: flammeus portwine sanguineous strawberry vascular NOS verrucous Excl.: café au lait spots (L81.3) lentigo (L81.4) naevus: NOS (D22.-) araneus (I78.1) melanocytic (D22.-) pigmented (D22.-) spider (I78.1) stellar (I78.1)
• Q82.8 Other specified congenital malformations of skin Abnormal palmar creases Accessory skin tags Benign familial pemphigus [Hailey-Hailey] Cutis laxa (hyperelastica) Dermatoglyphic anomalies Inherited keratosis palmaris et plantaris Keratosis follicularis [Darier-White] Excl.: Ehlers-Danlos syndrome (Q79.6)
• Q82.9 Congenital malformation of skin, unspecified

Q83 Congenital malformations of breast

Excl.: absence of pectoral muscle (Q79.8)

• Q83.0 Congenital absence of breast with absent nipple
• Q83.1 Accessory breast Supernumerary breast
• Q83.2 Absent nipple
• Q83.3 Accessory nipple Supernumerary nipple
• Q83.8 Other congenital malformations of breast Hypoplasia of breast
• Q83.9 Congenital malformation of breast, unspecified

Q84 Other congenital malformations of integument

• Q84.0 Congenital alopecia Congenital atrichosis
• Q84.1 Congenital morphological disturbances of hair, not elsewhere classified Beaded hair Monilethrix Pili annulati Excl.: Menkes' kinky hair syndrome (E83.0)
• Q84.2 Other congenital malformations of hair Congenital: hypertrichosis malformation of hair NOS Persistent lanugo
• Q84.3 Anonychia Excl.: nail patella syndrome (Q87.2)
• Q84.4 Congenital leukonychia
• Q84.5 Enlarged and hypertrophic nails Congenital onychauxis Pachyonychia
• Q84.6 Other congenital malformations of nails Congenital: clubnail koilonychia malformation of nail NOS
• Q84.8 Other specified congenital malformations of integument Aplasia cutis congenita
• Q84.9 Congenital malformation of integument, unspecified Congenital: anomaly NOS deformity NOS of integument NOS

Q85 Phakomatoses, not elsewhere classified

Excl.: ataxia telangiectasia [Louis-Bar] (G11.3) familial dysautonomia [Riley-Day] (G90.1)

• Q85.0 Neurofibromatosis (nonmalignant) Von Recklinghausen's disease
• Q85.1 Tuberous sclerosis Bourneville's disease Epiloia
• Q85.8 Other phakomatoses, not elsewhere classified Syndrome: Peutz-Jeghers Sturge-Weber(-Dimitri) von Hippel-Lindau Excl.: Meckel-Gruber syndrome (Q61.9)
• Q85.9 Phakomatosis, unspecified Hamartosis NOS

Dr Amanda Oakley

2010

Incomplete development of the nail of the hallux in the newborn

Dermatol Online J. 2010 Jun 15;16(6):1.

Milano A, Cutrone M, Laforgia N, Bonifazi E.

Unit of Paediatric Dermatology, University of Bari, Bari, Italy. Abstract Between March and October 2008, the nails of 541 (252 females, 289 males) consecutively born neonates with an average age of 3.2 days were examined in the Neonatology Unit. Of these newborns with nail disorders, 36 were re-examined after a period that ranged from seven days to six months. The most frequent nail alteration was the incomplete development of the hallux nail, which was triangular - sometimes trapezoidal - shaped. This alteration, which had been previously reported in the literature as congenital hypertrophy of the lateral folds of the hallux, spontaneously regressed within one to three months in the infants re-examined. There was no associated inflammation or onychocryptosis at any time. The apparent hypertrophy of the nail folds seemed to be secondary to the lack of pressure of the nail lamina.

PMID: 20579456

http://www.ncbi.nlm.nih.gov/pubmed/20579456

http://dermatology.cdlib.org/1606/1_originals/1_10-00107/bonifazi.html

Dermatology Online Journal was created in an effort to explore the educational potential of distributed hypermedia served via the World Wide Web. The journal is attempting to serve the dual role of providing relevant information and improving the way scholarly content is shared. Dermatology Online Journal © The Regents of the University of California, Davis campus. Individual articles © by their authors. All material is available under the Creative Commons BY-NC-ND license. This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License

Atopic dermatitis-like disease and associated lethal myeloproliferative disorder arise from loss of Notch signaling in the murine skin

Dumortier A, Durham AD, Di Piazza M, Vauclair S, Koch U, Ferrand G, Ferrero I, Demehri S, Song LL, Farr AG, Leonard WJ, Kopan R, Miele L, Hohl D, Finke D, Radtke F. PLoS One. 2010 Feb 18;5(2):e9258. PMID: 20174635

http://www.ncbi.nlm.nih.gov/pubmed/20174635

http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0009258