clinic

David A. Chappell, MD

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David A. Chappell, MD is a clinic that specializes in Concierge Endocrinology. The clinic is located in Petaluma, California. David A. Chappell, MD is known for housing expert physicians. David A. Chappell, MD offers all the services, treatments and procedures pertinent to the specialties mentioned above.

1 Doctor | Website
About David A. Chappell, MD

"In my concierge medicine practice, I will be able to focus on a patient’s overall healthcare needs, not just their endocrine issues. I will evaluate a patient’s full medical profile and symptomology to best treat the whole person…mind, body and spirit. The size of my practice is limited so I can devote more time to each patient. This practice change allows me to schedule up to 30 minutes for routine appointments and approximately 60 minutes for the annual exam. Appointments will start promptly, and I will be able to spend more time with you. If a problem requires extra time for evaluation, I will reasonably accommodate you to the best of my ability. Also, our communication will be enhanced though a patient-dedicated cell phone and email."

Address

141 Lynch Creek Way Suite A, Petaluma,
CA 94954

Modes of Payment

Card | Cash


Providers
David A. Chappell - 141 Lynch Creek Way, Petaluma, California, 94954
David A. Chappell, MD
Concierge Endocrinology
Fee $0 - $0
Max no. of Patients: N/A
Accepting New Patients: NA
141 Lynch Creek Way, Suite A, Petaluma, CA 94954

Reviews

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Conditions Treated
  • Diabetic ketoacidosis
  • Addison's disease
  • Adenomyosis
  • Thyroid cancer
  • Endometriosis
  • Thyroid eye disease
  • Uterine fibroids
  • Hypothyroidism
  • Hyperthyroidism
  • Type 2 diabetes
  • Type 1 diabetes
  • Osteoporosis
  • Ectopic pregnancy
  • Cushing syndrome
  • Ovarian cysts
  • Obesity
  • Diabetes
  • Graves' disease
  • Gestational diabetes
  • Atherosclerosis
  • Acromegaly
  • Androgen insensitivity syndrome
  • Apoplexy
  • Carcinoid syndrome
  • Congenital adrenal hyperplasia
  • Diabetes insipidus
  • Diabetes mellitus
  • Diabetic foot ulcers
  • Diabetic neuropathy
  • Diabetic retinopathy
  • Familial hypercholesterolemia
  • Fibrous dysplasia
  • Gigantism
  • Growth hormone deficiency
  • Hashimoto thyroiditis
  • High potassium level
  • Hyperaldosteronism
  • Hypercalcemia
  • Hyperparathyroidism
  • Hypogonadism
  • Hypoparathyroidism
  • Hypophosphatemia
  • Hypopituitarism
  • Kallmann syndrome
  • Low blood sugar
  • Low testosterone
  • Macrosomia
  • Magnesium deficiency
  • Malnutrition
  • Metabolic acidosis
  • Metabolic syndrome
  • Neuroendocrine tumor
  • Non alcoholic fatty liver disease
  • Noonan syndrome
  • Osteomalacia
  • Ovarian hyperstimulation syndrome
  • Papillary thyroid cancer
  • Phenylketonuria
  • Pheochromocytoma
  • Pituitary tumor
  • Precocious puberty
  • Prolactinoma
  • Rickets
  • Thyroid nodule
  • Thyroid storm
  • Thyroiditis
  • Xanthoma
  • Zollinger ellison syndrome
  • Abetalipoproteinemia
  • Adrenal cancer
  • Adrenal gland adenoma
  • Adrenocortical carcinoma
  • Albright's hereditary osteodystrophy
  • Alcoholic ketoacidosis
  • Alkaptonuria
  • Alstrom syndrome
  • Anaplastic thyroid cancer
  • Bardet biedl syndrome
  • Bartter syndrome
  • Congenital hyperinsulinism
  • Congenital hypothyroidism
  • Diabetic foot care
  • Diabetic macular edema
  • Diabetic nephropathy
  • Diabetic peripheral neuropathy
  • Empty sella syndrome
  • Female pattern baldness
  • Floating harbor syndrome
  • Follicular cyst of the ovary
  • Follicular thyroid cancer
  • Gitelman syndrome
  • Glucagonoma
  • Gonadal dysgenesis
  • Hirsutism in women
  • Hypervitaminosis d
  • Hypoaldosteronism
  • Hypogonadotropic hypogonadism
  • Insulinoma
  • Laron syndrome
  • Liddle syndrome
  • Low potassium level
  • Male infertility
  • Mccune albright syndrome
  • Medullary thyroid carcinoma
  • Milk alkali syndrome
  • Multiple endocrine neoplasia
  • Multiple endocrine neoplasia type 2
  • Nelson syndrome
  • Nephrocalcinosis
  • Nephrogenic diabetes insipidus
  • Newborn low blood sugar
  • Ornithine transcarbamylase deficiency
  • Panhypopituitarism
  • Parathyroid adenoma
  • Parathyroid cancer
  • Pituitary apoplexy
  • Pituitary dwarfism
  • Premature ovarian failure
  • Pseudohypoparathyroidism
  • Renal glycosuria
  • Secondary adrenal insufficiency
  • Short stature
  • Subacute thyroiditis
  • Swyer syndrome
  • Syndrome of inappropriate antidiuretic hormone secretion
  • Thyroid disorders
  • Weight management
  • Wolfram syndrome
  • Acute adrenal crisis
  • Apparent mineralocorticoid excess
  • Aromatase deficiency
  • Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy
  • Autoimmune polyglandular syndrome type 2
  • Breast enlargement in males
  • Delayed growth
  • Disorders of lipoid metabolism
  • Donohue syndrome
  • Ectopic cushing syndrome
  • Endocrinology and metabolism
  • Exogenous cushing syndrome
  • Familial combined hyperlipidemia
  • Familial hypertriglyceridemia
  • Familial hypobetalipoproteinemia
  • Familial partial lipodystrophy
  • Fanconi bickel syndrome
  • Female infertility
  • Galactokinase deficiency
  • Glucocorticoid remediable aldosteronism
  • Glucocorticoid resistance
  • Glycogen storage disease type 0
  • Glycogen storage disease type 3
  • Heterozygous familial hypercholesterolemia
  • Homozygous familial hypercholesterolemia
  • Hypoglycemic coma
  • Hypothalamic tumor
  • Idiopathic hypercalciuria
  • Leydig cell hypoplasia
  • Maturity onset diabetes of the young
  • Molybdenum cofactor deficiency
  • Multiple endocrine neoplasia type 1
  • Multiple symmetric lipomatosis
  • Neonatal hypothyroidism
  • Non toxic goiter
  • Osteitis fibrosa
  • Ovarian dysfunction
  • Overweight and obesity
  • Parathyroid hyperplasia
  • Partial androgen insensitivity syndrome
  • Pediatric obesity
  • Persistent mullerian duct syndrome
  • Pinealectomy
  • Primary angle closure glaucoma
  • Progressive osseous heteroplasia
  • Pseudohypoaldosteronism type 1
  • Puberty disorder
  • Pyruvate dehydrogenase deficiency
  • Rabson mendenhall syndrome
  • Russell silver dwarfism
  • Shapiro syndrome
  • Short chain acyl coa dehydrogenase deficiency
  • Short syndrome
  • Silent thyroiditis
  • Sitosterolemia
  • Somatostatinoma
  • Testicular failure
  • Thyroid dysgenesis
  • Thyrotoxic periodic paralysis
  • Toxic nodular goiter
  • Triple a syndrome
  • Very long chain acyl coa dehydrogenase deficiency
  • Wolcott rallison syndrome
  • Abdominal obesity metabolic syndrome
  • Acromegaloid facial appearance syndrome
  • Autosomal dominant hypocalcemia
  • Benign thyroid diseases
  • Carnitine acylcarnitine translocase deficiency
  • Carnitine palmitoyltransferase 1 deficiency
  • Childhood hypophosphatasia
  • Cold induced sweating syndrome
  • Congenital lipoid adrenal hyperplasia
  • Cushing syndrome due to adrenal tumor
  • Cytochrome p450 oxidoreductase deficiency
  • Diabetic hyperglycemic hyperosmolar syndrome
  • Diabetic kidney disorder
  • Essential pentosuria
  • Familial glucocorticoid deficiency
  • Familial hdl deficiency
  • Familial hyperaldosteronism
  • Familial hypertension
  • Familial hypopituitarism
  • Familial isolated hyperparathyroidism
  • Familial lipoprotein lipase deficiency
  • Fertility and conception
  • Fructose 1
  • Generalized resistance to thyroid hormone
  • Genital dwarfism
  • Glucose transporter deficiency
  • Granulomatous hypophysitis
  • Hereditary hypophosphatemic rickets
  • Hereditary paraganglioma pheochromocytoma syndrome
  • Hyperglycerolemia
  • Hyperlipidemia type 3
  • Hyperlipoproteinemia type 4
  • Hyperlipoproteinemia type 5
  • Hypolipoproteinemia
  • Infant hyperglycemia
  • Isolated acth deficiency
  • Isolated growth hormone deficiency
  • Isolated hypogonadotropic hypogonadism
  • Kenny caffey syndrome type 2
  • Long chain 3 hydroxyacyl coa dehydrogenase deficiency
  • Malonyl coa decarboxylase deficiency
  • Maternal hyperphenylalaninemia
  • Menopausal and postmenopausal disorders
  • Metastatic insulinoma
  • Methylmalonic acidemia with homocystinuria
  • Morgagni stewart morel syndrome
  • Multiple carboxylase deficiency
  • Neonatal severe hyperparathyroidism
  • Neurohypophyseal diabetes insipidus
  • Ornithine translocase deficiency
  • Osteoporosis pseudoglioma syndrome
  • Ovarian overproduction of androgens
  • Peroxisomal acyl coa oxidase deficiency
  • Pgm1 cdg
  • Pmm2 congenital disorder of glycosylation
  • Pseudohypoaldosteronism type 2
  • Rft1 cdg
  • Thyroid hormone plasma membrane transport defect
  • Transient neonatal diabetes mellitus
  • Type a insulin resistance syndrome
  • Type b insulin resistance syndrome
  • Weight control and obesity
more..
Treatments & Procedures
  • Hormone replacement therapy
  • Dexa scan
  • Bone density test
  • Blood glucose monitoring
  • Insulin treatment
  • Bone densitometry
  • Hormone treatments
  • Dietary counseling
  • Point of care a1c
Additional Services
  • Not available

Frequently Asked Questions

Where is David A. Chappell, MD located?

David A. Chappell, MD is located in 141 Lynch Creek Way Suite A, Petaluma, CA 94954.

What are the various modes of payment does David A. Chappell, MD Accept?

David A. Chappell, MD accepts Card | Cash.

What are the doctors who practice in David A. Chappell, MD specialize in?

Currently there are around 1 providers practice in David A. Chappell, MD who specialise in Concierge Endocrinology, etc

How can I make appointments with doctors in David A. Chappell, MD?

You can take appointments for doctors who practice in David A. Chappell, MD online on their website or by calling them.

Location