spondyloepiphyseal dysplasia congenita

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
A Natural History Study in Children With a Type II Collagen Disorder With Short Stature	Bone Diseases, Developmental, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dwarfism, Kniest dysplasia, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, Strudwick syndrome, bone disorder, connective tissue disorder, cutaneous mucinosis, endocrine system disorder, hereditary disease, hypochondrogenesis, inborn carbohydrate metabolic disorder, inborn errors of metabolism, lysosomal storage disease, metabolic disease, mucopolysaccharidosis, mucopolysaccharidosis type 4, musculoskeletal system disorder, spondyloepiphyseal dysplasia congenita	Recruiting	Not stated	2023-10-02		NCT05408715

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