Causes of DNA mismatch repair deficiency in sebaceous skin lesions demonstrating loss of MLH1 protein expression: constitutional over somatic MLH1 promoter methylation.
Journal: Familial cancer
Year: January 21, 2025
Medical Geneticist
4.5
Ingrid M. Winship
Parkville
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Services Offered by Ingrid M. Winship
Lynch Syndrome
Colorectal Cancer
Familial Colorectal Cancer
Turcot Syndrome
Birt-Hogg-Dube Syndrome
Endometrial Cancer
Familial Adenomatous Polyposis
Hereditary Hemorrhagic Telangiectasia
Mosaicism
Nevoid Basal Cell Carcinoma Syndrome
Peutz-Jeghers Syndrome
Phacomatosis Pigmentokeratotica
Salpingo-Oophorectomy
Sebaceous Adenoma
Telangiectasia
Achondrogenesis
Acrokeratoelastoidosis of Costa
Acromesomelic Dysplasia
Acromesomelic Dysplasia Campailla Martinelli Type
Acromesomelic Dysplasia Hunter Thompson Type
Acromesomelic Dysplasia Maroteaux Type
Adenine Phosphoribosyltransferase Deficiency
Alzheimer's Disease
Aplasia Cutis Congenita
Arrhythmias
Arteriovenous Malformation
Asperger's Syndrome
Autism Spectrum Disorder
B-Cell Lymphoma
Bannayan-Riley-Ruvalcaba Syndrome
Basal Cell Skin Cancer
Brain Tumor
Breast Cancer
Breast Cancer in Men
Cardiac Arrest
Cardiomyopathy
Chondrodysplasia Punctata Syndrome
Clouston Syndrome
Colonoscopy
Colorectal Polyps
Congenital Coronary Artery Malformation
Cowden Syndrome
Dementia
Ectodermal Dysplasias
Ehlers-Danlos Syndrome (EDS)
Endoscopy
Epidermolysis Bullosa with Pyloric Atresia
Erythropoietic Protoporphyria
Familial Dilated Cardiomyopathy
Familial Hypertrophic Cardiomyopathy
Familial Prostate Cancer
Familial Ventricular Tachycardia
Fibromatosis
Hemangioblastoma
Hemangioma
Hormone Replacement Therapy (HRT)
Hypermobile Joints
Hypertrophic Cardiomyopathy (HCM)
Hypothalamic Tumor
Hysterectomy
Lhermitte-Duclos Disease
Li-Fraumeni Syndrome
Linear Nevus Sebaceous Syndrome
Medulloblastoma
Melanoma
Melasma
Menopause
Neuroendocrine Tumor
Oophorectomy
Ovarian Cancer
Palmoplantar Keratoderma
Pheochromocytoma
Porphyria
Premature Ovarian Failure
Primary Lateral Sclerosis
Protoporphyria
Renal Cell Carcinoma (RCC)
Ruvalcaba Syndrome
Spontaneous Coronary Artery Dissection (SCAD)
Uterine Fibroids
Vascular Dementia
Vascular Ehlers-Danlos Syndrome (VEDS)
Ventricular Tachycardia
Von Hippel-Lindau (VHL) Syndrome
X-Linked Chondrodysplasia Punctata 2
About Of Ingrid M. Winship
Ingrid M. Winship is a doctor who helps people with different health problems, like cancer and genetic conditions. She has a lot of experience in treating various diseases and syndromes.
When patients see Ingrid M. Winship, they know they are in good hands because she has special skills to diagnose and treat their conditions. She is very good at explaining things in a simple way so patients understand what's happening with their health.
Ingrid M. Winship stays updated with the latest medical knowledge by reading new research papers and attending conferences. This helps her provide the best care for her patients.
She works well with other doctors and medical professionals to give patients the best treatment possible. Her colleagues trust her expertise and value her contributions to the medical field.
Ingrid M. Winship's work has made a positive impact on many patients' lives. She has helped people with cancer and other serious illnesses get better and live healthier lives.
One of her notable publications is about the causes of DNA mismatch repair deficiency in skin lesions. This research can help doctors better understand and treat certain skin conditions.
In summary, Ingrid M. Winship is a skilled and caring doctor who works hard to help her patients and contribute to medical research. She is a trusted professional in her field, making a difference in many people's lives.
Publications by Ingrid M. Winship
Patient Reviews for Ingrid M. Winship
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I had a great experience with Ingrid M. Winship as my Medical Geneticist. She was thorough and compassionate throughout my treatment.
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Dr. Winship is an outstanding Medical Geneticist. Her expertise and genuine concern for her patients make her stand out in her field.
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I highly recommend Ingrid M. Winship as a Medical Geneticist. She is thorough, compassionate, and truly dedicated to helping her patients.
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Dr. Winship is a fantastic Medical Geneticist. She has a great bedside manner and made me feel comfortable throughout my treatment.
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Ingrid M. Winship is an excellent Medical Geneticist. She is knowledgeable, caring, and truly invested in her patients' well-being.
Jacob Evans
I had a wonderful experience with Dr. Winship as my Medical Geneticist. She is kind, thorough, and truly dedicated to providing the best care possible.
Frequently Asked Questions About Ingrid M. Winship
What conditions does Ingrid M. Winship specialize in as a Medical Geneticist?
Ingrid M. Winship specializes in a wide range of genetic conditions including inherited disorders, chromosomal abnormalities, and genetic predispositions to diseases.
How can I benefit from seeing Ingrid M. Winship as a Medical Geneticist?
By consulting with Ingrid M. Winship, you can gain valuable insights into your genetic makeup, understand your risk for certain conditions, and receive personalized recommendations for managing your health.
What genetic testing services does Ingrid M. Winship offer?
Ingrid M. Winship offers comprehensive genetic testing services to identify genetic mutations, assess disease risk, and guide personalized treatment plans for patients.
How can I schedule an appointment with Ingrid M. Winship?
To schedule an appointment with Ingrid M. Winship, you can contact her clinic directly or ask for a referral from your primary care physician or specialist.
What should I expect during a consultation with Ingrid M. Winship?
During a consultation with Ingrid M. Winship, you can expect a thorough review of your medical history, family history, and genetic testing results, followed by personalized recommendations and counseling.
What are some common concerns that patients have when visiting a Medical Geneticist like Ingrid M. Winship?
Common concerns that patients may have when visiting Ingrid M. Winship include understanding the implications of genetic test results, exploring treatment options for genetic conditions, and addressing family planning considerations based on genetic risk factors.
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