Physician

Pathology

Dr. Felicitas L. Lacbawan, MD

Felicitas L. Lacbawan is an expert in the field of Pathology. She researched medicine at SUNY Upstate Medical University. Doctor Felicitas L. Lacbawan, MD is a published MD. She has 34 publications published. The most current publication "Is myoglobin useful in the diagnosis of acute myocardial infarction in the emergency department setting?" Doctor Felicitas L. Lacbawan, MD accepts all Medicare patients.

Publications

Improving Molecular Genetic Test Utilization through Order Restriction, Test Review, and Guidance.
Molecular testing for the BRCA1 and BRCA2 Ashkenazi Jewish founder mutations: a report on the College of American Pathologists proficiency testing surveys.
Institutional Profile: Cleveland Clinic's Center for Personalized Healthcare: setting the stage for value-based care.
Kuskokwim syndrome, a recessive congenital contracture disorder, extends the phenotype of FKBP10 mutations.
Verification of performance specifications of a molecular test: cystic fibrosis carrier testing using the luminex liquid bead array.
Brain-derived neurotrophic factor and obesity in the WAGR syndrome.
Central nervous system embryogenesis and its failures.
Mutations in the human SIX3 gene in holoprosencephaly are loss of function.
The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism.
Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans.
Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function.
A novel SIX3 mutation segregates with holoprosencephaly in a large family.
The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of th...
Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals.
Holoprosencephaly in a family segregating novel variants in ZIC2 and GLI2.
Unique phenotype in a patient with CHARGE syndrome.
Large interstitial deletion of chromosome 13q and severe short stature: clinical report and review of the literature.
A female infant with duplication of chromosome 2q33 to 2q37.3.
Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotype.
Functional analysis of mutations in TGIF associated with holoprosencephaly.
Abnormal sterol metabolism in holoprosencephaly: studies in cultured lymphoblasts.
Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literature.
Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly.
Additional EFNB1 mutations in craniofrontonasal syndrome.
Is myoglobin useful in the diagnosis of acute myocardial infarction in the emergency department setting?
Familial dementia caused by polymerization of mutant neuroserpin.
Rare interstitial deletion (2)(p11.2p13) in a child with pericentric inversion (2)(p11.2q13) of paternal origin.
Familial encephalopathy with neuroserpin inclusion bodies.
Severe hypodontia and oral xanthomas in Alagille syndrome.
Clinical heterogeneity in mitochondrial DNA deletion disorders: a diagnostic challenge of Pearson syndrome.
Pulmonary dysfunction in adults with nephropathic cystinosis.
Association between conformational mutations in neuroserpin and onset and severity of dementia.
Report of a child with aortic aneurysm, orofacial clefting, hemangioma, upper sternal defect, and marfanoid features: possible PHACE syndrome.

Schools

University of The Philippines System Institute of Health Science
University Philippines Philippine Genl Hospital
SUNY Health Science Center
NIH

Doctors Specialties

Molecular Genetic Pathology
Pathology

Accepted Insurances

Education

National Institutes of Health Clinical Center
SUNY Upstate Medical University
University of the Philippines College of Medicine

Hospital

Cleveland Clinic

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Medicare Facts

National Provider Identifier [NPI]	1518045822
Last Name Of The Provider	LACBAWAN
First Name Of The Provider	FELICITAS
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