Dr. Dorothy K Grange MD
Geneticist | Clinical Genetics (M.D.)
1 Childrens Pl Saint Louis MO, 63110Rating
3/5
About
Dr. Dorothy Grange practices Genetic Medicine in Saint Louis, MO. As a geneticist, Dr. Grange performs experiments and analyzes data to interpret the inheritance of different traits in patients. A geneticist evaluates, diagnoses, and manages patients with hereditary conditions or congenital malformations, genetic risk calculations, and mutation analysis. Dr. Grange carries out studies, tests, and counsels patients with genetic diseases.
Education and Training
Univ of Fl Coll of Med, Gainesville Fl 1981
University of Florida College of Medicine 1981
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG- Medical Biochemical Genetics
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- A patient with Ehlers-Danlos syndrome type VI is homozygous for a premature termination codon in exon 14 of the lysyl hydroxylase 1 gene.
- Fronto-otopalatodigital osteodysplasia: clinical evidence for a single entity encompassing Melnick-Needles syndrome, otopalatodigital syndrome types 1 and 2, and frontometaphyseal dysplasia.
- Preferential involvement of the short arm in chromosome 8-derived supernumerary
- Two unbalanced translocations involving a common 6p25 region in two XY female patients.
- Intracranial infantile myofibromatosis with intraparenchymal involvement.
- Case report: lethal multiple pterygium syndrome.
- Amino acid clearance during acute metabolic decompensation in maple syrup urine disease treated with continuous venovenous hemodialysis with filtration.
- New cases of Bohring-Opitz syndrome, update, and critical review of the literature.
- Increased progerin expression associated with unusual LMNA mutations causes severe progeroid syndromes.
- Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes.
- Response monitoring in children with phenylketonuria.
- IDH2 mutations in patients with D-2-hydroxyglutaric aciduria.
- Safety of extended treatment with sapropterin dihydrochloride in patients with phenylketonuria: results of a phase 3b study.
- Complex genomic rearrangement of chromosome 16p13.3 detected by array comparative genomic hybridization in a patient with multiple congenital anomalies, dysmorphic craniofacial features, and developmental delay.
- Tracking clinical genetic services for newborns identified through newborn dried bloodspot screening in the United States-lessons learned.
Treatments
- Birth Defects
- Down Syndrome
Dr. Dorothy K Grange MD's Practice location
Practice At 1 Childrens Pl
1 Childrens Pl -Saint Louis, MO 63110Get Direction
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Nearest Hospitals
SSM HEALTH SAINT LOUIS UNIVERSITY HOSPITALl
3635 VISTA AVE SAINT LOUIS MO 63110SHRINERS HOSPITALS FOR CHILDRENl
4400 CLAYTON AVE SAINT LOUIS MO 63110