autosomal recessive congenital ichthyosis 1

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Lymphocyte Phenotype of Autosomal Recessive Congenital Ichthyoses Mutated NIPAL4 (Nipal4-nEDD)	Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, Ichthyosiform Erythroderma, Congenital, Infant, Newborn, Diseases, Neoplasms by Histologic Type, Sezary syndrome, Skin Abnormalities, Skin and Connective Tissue Diseases, T-cell non-Hodgkin lymphoma, autosomal recessive congenital ichthyosis 1, hereditary disease, hereditary skin disorder, ichthyosis, immune system disorder, immunoproliferative disorder, keratosis, lymphatic system disorder, lymphoma, lymphoproliferative syndrome, neoplasm, primary cutaneous T-cell non-Hodgkin lymphoma, skin disorder	Not yet recruiting	Not stated	2026-03-17		NCT07477769

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