Crucial
It is feasible that the primary title of the record Keratitis Ichthyosis Deafness Syndrome is not the name you anticipated. Kindly examine the words noting to encounter the alternative name(s) as well as condition class(s) covered by this record.
Words
- Ichthyosiform Erythroderma, Corneal Involvement, and also Deafness Syndrome
- YOUNGSTER Syndrome
Condition Subdivisions
- None
General Discussion
Keratitis ichthyosis hearing problems (KID) disorder is an unusual, hereditary, multi-system problem. YOUNGSTER disorder belongs to a team of skin conditions noted by completely dry, flaky skin recognized as the ichthyoses.
Kenny-Caffey disorder kind 2 (KCS2) is an exceptionally uncommon genetic skeletal condition defined by thickening of the lengthy bones, slim marrow tooth cavities in the bones (medullary constriction), as well as problems impacting the head as well as eyes. Kenny-Caffey disorder kind 2 (KCS2) is an exceptionally uncommon genetic skeletal condition defined by thickening of the lengthy bones, slim marrow dental caries in the bones (medullary constriction), and also problems influencing the head as well as eyes. Kenny-Caffey disorder kind 2 (KCS2) is an incredibly unusual genetic skeletal condition defined by thickening of the lengthy bones, slim marrow dental caries in the bones (medullary constriction), and also irregularities influencing the head and also eyes. Keratitis ichthyosis hearing problems (KID) disorder is an uncommon, hereditary, multi-system condition. YOUNGSTER disorder belongs to a team of skin conditions noted by completely dry, flaky skin recognized as the ichthyoses.