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Dr. Stephen Kahler


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Office Location Physician Specialty Phone Number and Additional Info

Address:  
4301 W Markham St # 547-13
Little Rock, AR 72205

Medical Genetics
Clinical Genetics (M.D.), Pediatric Medical Genetics, Clinical Biochemical Genetics
Pediatrics
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qter and deletion of 18p11.32-->pter with mild phenotype: Patau syndrome and duplications of 13q revisited." ["pub_year"]=> string(4) "1996" ["pub_month"]=> string(2) "12" ["journal"]=> string(27) "Journal of medical genetics" } [40]=> array(5) { ["id"]=> string(7) "8817344" ["article"]=> string(77) "Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37." ["pub_year"]=> string(4) "1997" ["pub_month"]=> string(1) "1" ["journal"]=> string(24) "Human molecular genetics" } [41]=> array(5) { ["id"]=> string(7) "8891562" ["article"]=> string(130) "Acute pancreatitis in an infant with lactic acidosis and a mutation at nucleotide 3243 in the mitochondrial DNA tRNALeu(UUR) gene." ["pub_year"]=> string(4) "1997" ["pub_month"]=> string(1) "1" ["journal"]=> string(30) "European journal of pediatrics" } [42]=> array(5) { ["id"]=> string(7) "8880577" ["article"]=> string(83) "Double mutant fibrillin-1 (FBN1) allele in a patient with neonatal Marfan syndrome." ["pub_year"]=> string(4) "1997" ["pub_month"]=> string(1) "2" ["journal"]=> string(27) "Journal of medical genetics" } [43]=> array(5) { ["id"]=> string(7) "9870205" ["article"]=> string(117) "One-methyl group metabolism in non-ketotic hyperglycinaemia: mildly elevated cerebrospinal fluid homocysteine levels." ["pub_year"]=> string(4) "1999" ["pub_month"]=> string(1) "3" ["journal"]=> string(38) "Journal of inherited metabolic disease" } [44]=> array(5) { ["id"]=> string(8) "10457287" ["article"]=> string(25) "Galactosaemia in Chinese." ["pub_year"]=> string(4) "1999" ["pub_month"]=> string(1) "9" ["journal"]=> string(39) "Journal of paediatrics and child health" } [45]=> array(5) { ["id"]=> string(8) "10588840" ["article"]=> string(86) "Treatment of pyruvate carboxylase deficiency with high doses of citrate and aspartate." ["pub_year"]=> string(4) "1999" ["pub_month"]=> string(2) "12" ["journal"]=> string(36) "American journal of medical genetics" } [46]=> array(5) { ["id"]=> string(8) "10682306" ["article"]=> string(142) "Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders." ["pub_year"]=> string(4) "2000" ["pub_month"]=> string(1) "3" ["journal"]=> string(38) "Journal of inherited metabolic disease" } [47]=> array(5) { ["id"]=> string(8) "10680820" ["article"]=> string(48) "Acute hydrocephalus in nonketotic hyperglycemia." ["pub_year"]=> string(4) "2000" ["pub_month"]=> string(1) "3" ["journal"]=> string(9) "Neurology" } [48]=> array(5) { ["id"]=> string(8) "10894222" ["article"]=> string(85) "Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated families." ["pub_year"]=> string(4) "2000" ["pub_month"]=> string(1) "7" ["journal"]=> string(19) "Annals of neurology" } [49]=> array(5) { ["id"]=> string(8) "11032332" ["article"]=> string(117) "Acylcarnitines in plasma and blood spots of patients with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase defiency." ["pub_year"]=> string(4) "2001" ["pub_month"]=> string(1) "2" ["journal"]=> string(38) "Journal of inherited metabolic disease" } [50]=> array(5) { ["id"]=> string(8) "11391349" ["article"]=> string(59) "Hepatic storage of glycogen in Niemann-Pick disease type B." ["pub_year"]=> string(4) "2001" ["pub_month"]=> string(1) "7" ["journal"]=> string(25) "The Journal of pediatrics" } [51]=> array(5) { ["id"]=> string(8) "12406983" ["article"]=> string(114) "Comprehensive screening of urine samples for inborn errors of metabolism by electrospray tandem mass spectrometry." ["pub_year"]=> string(4) "2002" ["pub_month"]=> string(2) "11" ["journal"]=> string(18) "Clinical chemistry" } [52]=> array(5) { ["id"]=> string(8) "12402345" ["article"]=> string(107) "Molecular studies in mutase-deficient (MUT) methylmalonic aciduria: identification of five novel mutations." ["pub_year"]=> string(4) "2003" ["pub_month"]=> string(1) "1" ["journal"]=> string(14) "Human mutation" } [53]=> array(5) { ["id"]=> string(8) "12711738" ["article"]=> string(58) "The epidemiology of childhood cardiomyopathy in Australia." ["pub_year"]=> string(4) "2003" ["pub_month"]=> string(1) "4" ["journal"]=> string(35) "The New England journal of medicine" } [54]=> array(5) { ["id"]=> string(8) "12561056" ["article"]=> string(43) "Metabolic disorders and mental retardation." ["pub_year"]=> string(4) "2003" ["pub_month"]=> string(1) "8" ["journal"]=> string(74) "American journal of medical genetics. Part C, Seminars in medical genetics" } [55]=> array(5) { ["id"]=> string(8) "14555645" ["article"]=> string(83) "A knock-out mouse model for methylmalonic aciduria resulting in neonatal lethality." ["pub_year"]=> string(4) "2004" ["pub_month"]=> string(1) "2" ["journal"]=> string(35) "The Journal of biological chemistry" } [56]=> array(5) { ["id"]=> string(8) "15810001" ["article"]=> string(121) "A novel MGP mutation in a consanguineous family: review of the clinical and molecular characteristics of Keutel syndrome." ["pub_year"]=> string(4) "2005" ["pub_month"]=> string(1) "5" ["journal"]=> string(44) "American journal of medical genetics. Part A" } [57]=> array(5) { ["id"]=> string(8) "16644012" ["article"]=> string(34) "Autism and environmental genomics." ["pub_year"]=> string(4) "2006" ["pub_month"]=> string(2) "10" ["journal"]=> string(15) "Neurotoxicology" } [58]=> array(5) { ["id"]=> string(8) "18553514" ["article"]=> string(130) "Native American myopathy: congenital myopathy with cleft palate, skeletal anomalies, and susceptibility to malignant hyperthermia." ["pub_year"]=> string(4) "2008" ["pub_month"]=> string(1) "8" ["journal"]=> string(44) "American journal of medical genetics. Part A" } [59]=> array(5) { ["id"]=> string(8) "18843099" ["article"]=> string(87) "Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1." ["pub_year"]=> string(4) "2008" ["pub_month"]=> string(2) "12" ["journal"]=> string(9) "Neurology" } [60]=> array(5) { ["id"]=> string(8) "19188198" ["article"]=> string(110) "Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes." ["pub_year"]=> string(4) "2009" ["pub_month"]=> string(1) "9" ["journal"]=> string(27) "Journal of medical genetics" } [61]=> array(3) { ["id"]=> string(8) "21519954" ["article"]=> string(107) "Metabolic imbalance associated with methylation dysregulation and oxidative damage in children with autism." 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This is an amazing doctor who is always happy and friendly. While you may have to wait a considerable time to see him when you go for a visit, the wait is due to the fact that he spends so much time with each patient and is so thorough and makes to sure to answer each question with accuracy(during one visit with my son he made a phone call to a physician at NIH in Bethesda, MD to make sure what he was telling me was accurate) that to us it is well worth the wait. I highly reccomend him to anyone with genetic issues." 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["worst"]=> string(1) "1" } } } } } ["wait_time"]=> string(2) "40" } } ["highlight"]=> string(58) "Patients' Choice,Rated 4 stars by patients,Board certified" ["mesh_expertise_set"]=> array(10) { [0]=> array(6) { ["expertise"]=> string(22) "Multiple Abnormalities" ["mesh_id"]=> string(2) "16" ["descriptor_name"]=> string(22) "Multiple Abnormalities" ["parent_mesh_id"]=> string(4) "8977" ["parent_tree_number"]=> string(3) "C16" ["parent_descriptor_name"]=> string(63) "Congenital, Hereditary, and Neonatal Diseases and Abnormalities" } [1]=> array(6) { ["expertise"]=> string(38) "Inborn Errors of Amino Acid Metabolism" ["mesh_id"]=> string(3) "567" ["descriptor_name"]=> string(38) "Inborn Errors of Amino Acid Metabolism" ["parent_mesh_id"]=> string(4) "9360" ["parent_tree_number"]=> string(3) "C18" ["parent_descriptor_name"]=> string(34) "Nutritional and Metabolic Diseases" } [2]=> array(6) { ["expertise"]=> string(22) "Chromosome Aberrations" ["mesh_id"]=> string(4) "2755" ["descriptor_name"]=> string(22) "Chromosome Aberrations" ["parent_mesh_id"]=> string(5) "13039" ["parent_tree_number"]=> string(3) "C23" ["parent_descriptor_name"]=> string(43) "Pathological Conditions, Signs and Symptoms" } [3]=> array(6) { ["expertise"]=> string(18) "Mental Retardation" ["mesh_id"]=> string(4) "8259" ["descriptor_name"]=> string(18) "Mental Retardation" ["parent_mesh_id"]=> string(5) "13039" ["parent_tree_number"]=> string(3) "C23" ["parent_descriptor_name"]=> string(43) "Pathological Conditions, Signs and Symptoms" } [4]=> array(6) { ["expertise"]=> string(18) "Mental Retardation" ["mesh_id"]=> string(4) "8259" ["descriptor_name"]=> string(18) "Mental Retardation" ["parent_mesh_id"]=> string(4) "1455" ["parent_tree_number"]=> string(3) "F03" ["parent_descriptor_name"]=> string(16) "Mental Disorders" } [5]=> array(6) { ["expertise"]=> string(54) "Inherited Metabolism Diseases Inborn Metabolism Errors" ["mesh_id"]=> string(4) "8311" ["descriptor_name"]=> string(26) "Metabolism (Inborn Errors)" ["parent_mesh_id"]=> string(4) "9360" ["parent_tree_number"]=> string(3) "C18" ["parent_descriptor_name"]=> string(34) "Nutritional and Metabolic Diseases" } [6]=> array(6) { ["expertise"]=> string(20) "Chromosome Disorders" ["mesh_id"]=> string(5) "19769" ["descriptor_name"]=> string(20) "Chromosome Disorders" ["parent_mesh_id"]=> string(4) "8977" ["parent_tree_number"]=> string(3) "C16" ["parent_descriptor_name"]=> string(63) "Congenital, Hereditary, and Neonatal Diseases and Abnormalities" } [7]=> array(6) { ["expertise"]=> string(18) "Mental Retardation" ["mesh_id"]=> string(4) "8259" ["descriptor_name"]=> string(18) "Mental Retardation" ["parent_mesh_id"]=> string(4) "9040" ["parent_tree_number"]=> string(3) "C10" ["parent_descriptor_name"]=> string(23) "Nervous System Diseases" } [8]=> array(6) { ["expertise"]=> string(38) "Inborn Errors of Amino Acid Metabolism" ["mesh_id"]=> string(3) "567" ["descriptor_name"]=> string(38) "Inborn Errors of Amino Acid Metabolism" ["parent_mesh_id"]=> string(4) "8977" ["parent_tree_number"]=> string(3) "C16" ["parent_descriptor_name"]=> string(63) "Congenital, Hereditary, and Neonatal Diseases and Abnormalities" } [9]=> array(6) { ["expertise"]=> string(54) "Inherited Metabolism Diseases Inborn Metabolism Errors" ["mesh_id"]=> string(4) "8311" ["descriptor_name"]=> string(26) "Metabolism (Inborn Errors)" ["parent_mesh_id"]=> string(4) "8977" ["parent_tree_number"]=> string(3) "C16" ["parent_descriptor_name"]=> string(63) "Congenital, Hereditary, and Neonatal Diseases and Abnormalities" } } ["feedback_questions"]=> array(1) { ["feedback"]=> array(8) { [0]=> array(2) { ["question"]=> string(30) "Ease in getting an appointment" ["id"]=> string(1) "1" } [1]=> array(2) { ["question"]=> string(27) "Waiting time during a visit" ["id"]=> string(1) "2" } [2]=> array(2) { ["question"]=> string(45) "Courtesy and professionalism of office staff " ["id"]=> string(1) "3" } [3]=> array(2) { ["question"]=> string(32) "Accuracy in diagnosing a problem" ["id"]=> string(1) "4" } [4]=> array(2) { ["question"]=> string(23) "Bedside manner (caring)" ["id"]=> string(1) "5" } [5]=> array(2) { ["question"]=> string(28) "Spending enough time with me" ["id"]=> string(1) "6" } [6]=> array(2) { ["question"]=> string(37) "Following up as needed after my visit" ["id"]=> string(1) "7" } [7]=> array(2) { ["question"]=> string(36) "How long was your wait at the office" ["id"]=> string(1) "8" } } } ["display_name_stripped"]=> string(16) "Stephen G Kahler" ["comment_count"]=> string(1) "2" ["highlight_meta_desc"]=> string(64) "Winner of Patients' Choice Award, Attended 4 Star Medical School" ["provider_standing_code"]=> string(1) "P" ["pca_year"]=> string(20) "20082012201020092011" ["awards_short"]=> string(63) "PCA 5th Anniversary,Patients' Choice Award,Compassionate Doctor" } --> Dr Stephen G Kahler, MD 's Report Card
Each year doctors receive positive patient ratings and win awards. They may continue their education, change their phone number and office location, or even add an additional address to their practice. We provide up-to-date information and patient reviews on Dr. Kahler, Pediatrician, and offer insight into why he has been listed as Patients' Choice Award recipient.
Doctors' Patient Ratings

based on 6 ratings
Overall Distribution
Ease of Appointment
 
3.0
Promptness
 
2.3
Courteous Staff
 
3.8
Accurate Diagnosis
 
3.0
Bedside Manner
 
3.5
Spends Time with Me
 
4.0
Follow Up
 
2.5
Board Certified Pediatrician
Doctor Reviews
Sanctions Found
NONE
Years Experience
36
Awards
7
Compassionate Doctor Recognition, 2012
Doctor Reviews
Patients' Choice Award, 2012
Doctor Reviews
Patients' Choice 5th Anniversary Award, 2012
Doctor Reviews
Patients' Choice Award, 2008 - 2011
Doctor Reviews

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  Highlights about Dr. Stephen Kahler
  • Patients' Choice
  • Rated 4 stars by patients
  • Board certified
  • Dr Stephen Kahler, has an overall rating of 4 stars out of 6 reviews
  • Gender: Male