Keratitis-ichthyosis-deafness (KID) syndrome

Dermatology Online Journal

Volumn 15, Issue 8, 2009, Pages

  Gonzalez, Mercedes E ^a   Tlougan, Brook E ^a   Price, Harper N ^a   Patel, Rishi ^a   Kamino, Hideko ^a   Schaffer, Julie V ^a  

^a NEW YORK UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CIPROFLOXACIN; CONNEXIN 26; COTRIMOXAZOLE; DOXYCYCLINE;

ADULT; ANTIBIOTIC THERAPY; ARTICLE; CASE REPORT; CODON; CONJUNCTIVA DISEASE; DERMIS; DRY EYE; HAIR FOLLICLE; HEARING AID; HUMAN; HUMAN TISSUE; HYPERKERATOSIS; ICHTHYOSIS; KERATOCONJUNCTIVITIS; KERATODERMA; LYMPHOCYTE; MALE; MISSENSE MUTATION; MOUTH PLAQUE; NAIL DYSTROPHY; NEUTROPHIL; PARAKERATOSIS; PERCEPTION DEAFNESS; PUS; RECURRENT INFECTION; SCALP; SERUM; SKIN INFECTION; SKIN NODULE; SYNDROME KID; VISUAL ACUITY; HEARING IMPAIRMENT; KERATITIS; PATHOLOGY; SYNDROME;

DEAFNESS; HUMANS; ICHTHYOSIS; KERATITIS; MALE; SYNDROME; YOUNG ADULT;

EID: 70349179277     PISSN: None     EISSN: 10872108     Source Type: Journal    
DOI: None     Document Type: Article

References (10)

1. Caceres-Rios H, et al. Keratitis, ichthyosis, and deafness (KID syndrome): review of the literature and proposal of a new terminology. Pediatr Dermatol 1996; 13: 105 [PubMed] (Pubitemid 26131955)
2. Skinner BA, et al. The keratitis, ichthyosis, and deafness (KID) syndrome. Arch Dermatol 1981; 117: 285 [PubMed]
3. Lazic T, et al. A report of GJB2 (N14K) connexin 26 mutation in two patients: a new subtype of KID syndrome. Pediatr Dermatol 2008; 25: 535 [PubMed]
4. Zhang XB. A case of keratitis ichthyosis deafness (KID) syndrome associated with Dandy-Walker. J Eur Acad Dermatol Venereol 2007; 21: 681 [PubMed]
5. Mazereeuw-Hautier J, et al. Keratitis-ichthyosis-deafness syndrome: disease expression and spectrum of connexin 26 (GjB2) mutations in 14 patients. Br J Dermatol 2007; 156: 1015 [PubMed] (Pubitemid 46642846)
6. Montgomery JR, et al. A novel connexin 26 gene mutation associated with features of the keratitis-ichthyosis-deafness syndrome and the follicular occlusion triad. J Am Acad Dermatol 2004; 51: 377 [PubMed]
7. Nyquist G, et al. Malignant proliferating pilar tumors arising in KID syndrome: a report of two patients. Am J Med Genet 2007; 143A: 734 [PubMed] (Pubitemid 46606684)
8. Kim KH, et al. Keratitis, ichthyosis and deafness syndrome with development of multiple hair follicle tumours. Br J Dermatol 2002; 147: 139 [PubMed]
9. Jan AY, et al. Genetic heterogeneity of KID syndrome: identification of a Cx30 gene (GJB6) mutation in a patient with KID syndrome and congenital atrichia. J Invest Dermatol 2004; 122: 1108 [PubMed]
10. Zhang X, et al. Severe ichthyosis-related disorders in children: response to acitretin. J Derm Treat 2007; 18: 118 [PubMed] (Pubitemid 46801839)