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
Dr. Dorothy K Grange MD's reviews
Write ReviewPatient Experience with Dr. Grange
Recommended Articles
![]()
Is Pancreatic Cancer Genetic?Is Pancreatic Cancer Genetic?Cancer is caused by a change in your genetic sequence. Genes are responsible for designing your body. Any alteration at that level will alter your body patterns.Cancer is an uncontrolled production of abnormal cells. Usually new cells are formed when your body needs...
![]()
Different Types of Physicians ExplainedDoctors or physicians are categorized according to different factors including medical specialties and subspecialties. Most doctors specialize in a specific area of medicine. This article provides a summary of the different types of doctors in the medical field. AllergistsAllergists are also...
![]()
What is Neurofibromatosis?Neurofibromatosis is a genetic disorder that affects the development of nerve cells and tissues in the body, leading to the formation of tumors in different parts of the nervous system. These tumors, also known as neurofibromas, may develop in the brain, spinal cord, along the nerves, or under the...
![]()
The Function and Structure of DNADeoxyribonucleic acid or DNA is a molecule that contains the instructions an organism needs to develop, live and reproduce. These instructions are found inside every cell and are passed down from parents to their children.The Structure of DNADNA contains molecules called nucleotides, which possess a...
![]()
What Is Pituitary Dwarfism?IntroductionPituitary dwarfism, also called growth hormone deficiency, is a medical condition wherein the pituitary gland does not produce sufficient amounts of growth hormone. This deficiency often results in children’s slow growth or short stature.An adult with pituitary dwarfism has an average...
![]()
The History of Muscular DystrophyWhat is muscular dystrophy?Muscular dystrophy is an inherited disorder, which is often characterized by a progressive type of muscular degeneration and weakness. There are several types of muscular dystrophy, wherein each type eventually leads to an increased disability, strength loss, and potential...
Nearby Providers
![]()
Stephen Braddock1465 S Grand Blvd, Division of Medical Genetics Saint Louis Missouri 63104![]()
Dr. Thomas Matthew Morgan MD1 Childrens Pl Saint Louis MO 63110![]()
Dr. Rick A Martin MD1 Childrens Pl Saint Louis MO 63110![]()
Dr. Jeffrey Milbrandt M.D.660 S Euclid Ave Saint Louis MO 63110![]()
Dr. James P Crane MD660 S Euclid Ave Saint Louis MO 63110![]()
Dr. Diana Lee Gray MD4921 Parkview Pl Saint Louis MO 63110
Nearest Hospitals
SHRINERS HOSPITALS FOR CHILDRENl
4400 CLAYTON AVE SAINT LOUIS MO 63110SSM HEALTH SAINT LOUIS UNIVERSITY HOSPITALl
3635 VISTA AVE SAINT LOUIS MO 63110