A very rare disorder where an infant is born covered with a transparent membrane which sheds to reveal large dark, plate-like scales. Type 3 is distinguished by the location of the genetic defect - chromosome 19p12-q12. This type also affects the ears and face to a greater degree than other types.
* Scaly skin * Colloidon membrane at birth * Upturned eyelids * Heat intolerance * Sparse eyebrows * Everted lower lip * Sparse scalp hair * Thin skin * Inelastic skin * Excessive nail growth * Scarring alopecia * Tight skin * Impaired finger mobility * Pruritus
signs and symptoms for Lamellar ichthyosis, type 3 has been gathered from various sources, may not be fully accurate, and may not be the full list of Lamellar ichthyosis, type 3 signs or Lamellar ichthyosis, type 3 symptoms. Furthermore, signs and symptoms of Lamellar ichthyosis, type 3 may vary on an individual basis for each patient. Only your doctor can provide adequate diagnosis of any signs or symptoms and whether they are indeed Lamellar ichthyosis, type 3 symptoms.