D
Diana García-Cruz
Researcher at University of Guadalajara
Publications - 48
Citations - 335
Diana García-Cruz is an academic researcher from University of Guadalajara. The author has contributed to research in topics: Trisomy & Camptodactyly. The author has an hindex of 9, co-authored 46 publications receiving 318 citations.
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Journal ArticleDOI
Inherited hypertrichoses: Inherited hypertrichoses
TL;DR: The review of generalized hypertrichoses from a historical point of view, including a review of their clinical and genetic features, shows heterogeneity with at least nine different entities.
Journal Article
Osteopoikilosis : report of a familial case
TL;DR: Four members of a family are described in which the clinical and radiological findings lead to consider the diagnosis of osteopoikilosis, and none of the subjects showed the skin lesions reported in the Buschke-Ollendorff syndrome.
Journal ArticleDOI
The Myhre syndrome: report of two cases.
Diana García-Cruz,Luis E. Figuera,A. Feria-Velazco,José Sánchez-Corona,M. O. García-Cruz,R. M. Ramirez-Duenãs,A. Hernandez-Córdova,M. X. Ruiz,W. E. Bitar-Alatorre,María de Lourdes Ramírez-Dueñas,J. M. Cantú +10 more
TL;DR: The Myhre syndrome: report of two cases of unexplained sudden death in children under the age of five.
Journal ArticleDOI
Guadalajara camptodactyly syndrome. A distinct probably autosomal recessive disorder.
TL;DR: Two sisters, aged 18 and 11 years, were found to have an intrauterine growth retardaion‐malformation syndrome which included camptodactyly as a typical sign and the family data suggested autosomal recessive inheritance.
Journal Article
Tetrasomy 9p: clinical aspects and enzymatic gene dosage expression.
Diana García-Cruz,Vaca G,Bertha Ibarra,José Sánchez-Corona,R Ocampo-Campos,S Peregrina,Moller M,Horacio Rivera,Fernando Rivas,A González-Angulo,J. M. Cantú +10 more
TL;DR: Biochemical studies corroborate the gene dosage effect for galactose-1-phosphate uridyltransferase and roentgenological findings were quite similar to those of the 9p trisomy except for hypoplastic and angulated ribs, and malformed vertebral bodies, which are probably exclusive of the tetrasomic state.