Kyphoscoliotic type of Ehlers-Danlos Syndrome (EDS VIA) in six Egyptian patients presenting with a homogeneous clinical phenotype.
Abdalla, Ebtesam M
Kyphoscoliotic type of Ehlers-Danlos Syndrome (EDS VIA) in six Egyptian patients presenting with a homogeneous clinical phenotype. [electronic resource] - European journal of pediatrics Jan 2015 - 105-12 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1432-1076
10.1007/s00431-014-2429-9 doi
Child
Child, Preschool
Craniofacial Abnormalities--etiology
Ehlers-Danlos Syndrome--diagnosis
Female
Humans
Infant
Male
Phenotype
Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase--deficiency
Kyphoscoliotic type of Ehlers-Danlos Syndrome (EDS VIA) in six Egyptian patients presenting with a homogeneous clinical phenotype. [electronic resource] - European journal of pediatrics Jan 2015 - 105-12 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1432-1076
10.1007/s00431-014-2429-9 doi
Child
Child, Preschool
Craniofacial Abnormalities--etiology
Ehlers-Danlos Syndrome--diagnosis
Female
Humans
Infant
Male
Phenotype
Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase--deficiency