- congenital ichthyosiform erythroderma
- Erythroderma n ichthyosiforme congenitum
Fachwörterbuch Medizin Englisch-Deutsch. 2013.
Fachwörterbuch Medizin Englisch-Deutsch. 2013.
Congenital ichthyosiform erythroderma — Classification and external resources ICD 10 Q80.2 ICD 9 757.1 … Wikipedia
nonbullous congenital ichthyosiform erythroderma — a genetically heterogeneous, autosomal recessive condition characterized by erythroderma and fine, white, semiadherent scales; other features include palmoplantar hyperkeratosis, nail dystrophy, and sparse hair. Most infants present as collodion… … Medical dictionary
Congenital lymphedema — is a blockage of fluid in the developing fetal lymphatic system. It is diagnosed by a nuchal scan. Presence of this condition is also associated with congenital heart defect.[1] See also Amniotic band syndrome HNRPH1 Norman Roberts syndrome… … Wikipedia
erythroderma — A nonspecific designation for intense and usually widespread reddening of the skin from dilation of blood vessel s, often preceding, or associated with exfoliation. SYN: erythrodermatitis. [erythro + G. derma, skin] bullous congenital… … Medical dictionary
List of cutaneous conditions — This is an incomplete list, which may never be able to satisfy particular standards for completeness. You can help by expanding it with reliably sourced entries. See also: Cutaneous conditions, Category:Cutaneous conditions, and ICD 10… … Wikipedia
Epidermolytic hyperkeratosis — Classification and external resources ICD 10 Q80.3 OMIM 113800 Diseases … Wikipedia
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
Lamellar ichthyosis — Ichthyosis lamellaris Classification and external resources ICD 10 Q80.2 OMIM 242300 DiseasesDB … Wikipedia
Zunich–Kaye syndrome — Zunich Kaye syndrome Classification and external resources ICD 10 GroupMajor.minor ICD 9 xxx … Wikipedia
Keratin 1 — is a member of the keratin family. It is specifically expressed in the spinous and granular layers of the epidermis with family member keratin 10. Mutations in this gene have been associated with the variants of bullous congenital ichthyosiform… … Wikipedia
Ichthyosis — Classification and external resources Ichthyosis is recognized by rough, scaly skin exhibited by patients. ICD 10 Q … Wikipedia