clinic

David A. Chappell, MD

5 Stars (6 Reviews)

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
Posted by FMDD User
May 19, 2024
Always calm and approachable. Never rushes through appointments.

Review For David A. Chappell

Posted by FMDD User
December 11, 2023

Review For David A. Chappell

Posted by FMDD User
March 12, 2024

Review For David A. Chappell

Posted by FMDD User
April 23, 2024

Review For David A. Chappell


Conditions Treated
  • Thyroid cancer
  • Familial hypercholesterolemia
  • Metabolic syndrome
  • Noonan syndrome
  • Diabetic neuropathy
  • Hypopituitarism
  • Pituitary tumor
  • Prolactinoma
  • Carcinoid syndrome
  • Malnutrition
  • Neuroendocrine tumor
  • Non alcoholic fatty liver disease
  • Zollinger ellison syndrome
  • Abetalipoproteinemia
  • Fibrous dysplasia
  • Acromegaly
  • Androgen insensitivity syndrome
  • Apoplexy
  • Congenital adrenal hyperplasia
  • Diabetes insipidus
  • Diabetes mellitus
  • Diabetic foot ulcers
  • Diabetic retinopathy
  • Gigantism
  • Growth hormone deficiency
  • Hashimoto thyroiditis
  • High potassium level
  • Hyperaldosteronism
  • Hypercalcemia
  • Hyperparathyroidism
  • Hypogonadism
  • Hypoparathyroidism
  • Hypophosphatemia
  • Kallmann syndrome
  • Low blood sugar
  • Low testosterone
  • Macrosomia
  • Magnesium deficiency
  • Metabolic acidosis
  • Osteomalacia
  • Ovarian hyperstimulation syndrome
  • Papillary thyroid cancer
  • Phenylketonuria
  • Pheochromocytoma
  • Precocious puberty
  • Rickets
  • Thyroid nodule
  • Thyroid storm
  • Thyroiditis
  • Xanthoma
  • Adrenal cancer
  • Adrenal gland adenoma
  • Adrenocortical carcinoma
  • Albright's hereditary osteodystrophy
  • Alcoholic ketoacidosis
  • Alkaptonuria
  • Diabetes
  • Atherosclerosis
  • Diabetic ketoacidosis
  • Type 2 diabetes
  • Obesity
  • Osteoporosis
  • Addison's disease
  • Adenomyosis
  • Thyroid eye disease
  • Uterine fibroids
  • Hypothyroidism
  • Hyperthyroidism
  • Type 1 diabetes
  • Ectopic pregnancy
  • Cushing syndrome
  • Ovarian cysts
  • Graves' disease
  • Gestational diabetes
  • Endometriosis
  • Female pattern baldness
  • Hirsutism in women
  • Hypervitaminosis d
  • Mccune albright syndrome
  • Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy
  • Familial partial lipodystrophy
  • Shapiro syndrome
  • Alstrom syndrome
  • Anaplastic thyroid cancer
  • Bardet biedl syndrome
  • Bartter syndrome
  • Congenital hyperinsulinism
  • Congenital hypothyroidism
  • Hypogonadotropic hypogonadism
  • Low potassium level
  • Multiple endocrine neoplasia
  • Multiple endocrine neoplasia type 2
  • Nelson syndrome
  • Panhypopituitarism
  • Secondary adrenal insufficiency
  • Syndrome of inappropriate antidiuretic hormone secretion
  • Apparent mineralocorticoid excess
  • Autoimmune polyglandular syndrome type 2
  • Maturity onset diabetes of the young
  • Overweight and obesity
  • Primary angle closure glaucoma
  • Pseudohypoaldosteronism type 1
  • Rabson mendenhall syndrome
  • Silent thyroiditis
  • Toxic nodular goiter
  • Abdominal obesity metabolic syndrome
  • Cold induced sweating syndrome
  • Diabetic hyperglycemic hyperosmolar syndrome
  • Diabetic kidney disorder
  • Familial isolated hyperparathyroidism
  • Generalized resistance to thyroid hormone
  • Granulomatous hypophysitis
  • Isolated acth deficiency
  • Floating harbor syndrome
  • Gitelman syndrome
  • Gonadal dysgenesis
  • Laron syndrome
  • Ornithine transcarbamylase deficiency
  • Swyer syndrome
  • Wolfram syndrome
  • Aromatase deficiency
  • Disorders of lipoid metabolism
  • Donohue syndrome
  • Familial combined hyperlipidemia
  • Familial hypertriglyceridemia
  • Familial hypobetalipoproteinemia
  • 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
  • Leydig cell hypoplasia
  • Molybdenum cofactor deficiency
  • Multiple endocrine neoplasia type 1
  • Multiple symmetric lipomatosis
  • Partial androgen insensitivity syndrome
  • Persistent mullerian duct syndrome
  • Pyruvate dehydrogenase deficiency
  • Russell silver dwarfism
  • Short chain acyl coa dehydrogenase deficiency
  • Short syndrome
  • Sitosterolemia
  • Thyroid dysgenesis
  • Triple a syndrome
  • Very long chain acyl coa dehydrogenase deficiency
  • Wolcott rallison syndrome
  • Acromegaloid facial appearance syndrome
  • Autosomal dominant hypocalcemia
  • Carnitine acylcarnitine translocase deficiency
  • Carnitine palmitoyltransferase 1 deficiency
  • Congenital lipoid adrenal hyperplasia
  • Cytochrome p450 oxidoreductase deficiency
  • Essential pentosuria
  • Familial glucocorticoid deficiency
  • Familial hdl deficiency
  • Familial hyperaldosteronism
  • Familial hypopituitarism
  • Familial lipoprotein lipase deficiency
  • Fructose 1
  • Genital dwarfism
  • Glucose transporter deficiency
  • Hereditary paraganglioma pheochromocytoma syndrome
  • Hyperglycerolemia
  • Isolated hypogonadotropic hypogonadism
  • Kenny caffey syndrome type 2
  • Long chain 3 hydroxyacyl coa dehydrogenase deficiency
  • Malonyl coa decarboxylase deficiency
  • Maternal hyperphenylalaninemia
  • Methylmalonic acidemia with homocystinuria
  • Morgagni stewart morel syndrome
  • Multiple carboxylase deficiency
  • Ornithine translocase deficiency
  • Peroxisomal acyl coa oxidase deficiency
  • Pgm1 cdg
  • Pmm2 congenital disorder of glycosylation
  • Rft1 cdg
  • Thyroid hormone plasma membrane transport defect
  • Type a insulin resistance syndrome
  • Type b insulin resistance syndrome
  • Diabetic foot care
  • Diabetic macular edema
  • Diabetic nephropathy
  • Diabetic peripheral neuropathy
  • Empty sella syndrome
  • Follicular cyst of the ovary
  • Follicular thyroid cancer
  • Glucagonoma
  • Hypoaldosteronism
  • Insulinoma
  • Liddle syndrome
  • Male infertility
  • Medullary thyroid carcinoma
  • Milk alkali syndrome
  • Nephrocalcinosis
  • Nephrogenic diabetes insipidus
  • Newborn low blood sugar
  • Parathyroid adenoma
  • Parathyroid cancer
  • Pituitary apoplexy
  • Pituitary dwarfism
  • Premature ovarian failure
  • Pseudohypoparathyroidism
  • Renal glycosuria
  • Short stature
  • Subacute thyroiditis
  • Thyroid disorders
  • Weight management
  • Acute adrenal crisis
  • Breast enlargement in males
  • Delayed growth
  • Ectopic cushing syndrome
  • Endocrinology and metabolism
  • Exogenous cushing syndrome
  • Hypoglycemic coma
  • Hypothalamic tumor
  • Idiopathic hypercalciuria
  • Neonatal hypothyroidism
  • Non toxic goiter
  • Osteitis fibrosa
  • Ovarian dysfunction
  • Parathyroid hyperplasia
  • Pediatric obesity
  • Pinealectomy
  • Progressive osseous heteroplasia
  • Puberty disorder
  • Somatostatinoma
  • Testicular failure
  • Thyrotoxic periodic paralysis
  • Benign thyroid diseases
  • Childhood hypophosphatasia
  • Cushing syndrome due to adrenal tumor
  • Familial hypertension
  • Fertility and conception
  • Hereditary hypophosphatemic rickets
  • Hyperlipidemia type 3
  • Hyperlipoproteinemia type 4
  • Hyperlipoproteinemia type 5
  • Hypolipoproteinemia
  • Infant hyperglycemia
  • Isolated growth hormone deficiency
  • Menopausal and postmenopausal disorders
  • Metastatic insulinoma
  • Neonatal severe hyperparathyroidism
  • Neurohypophyseal diabetes insipidus
  • Osteoporosis pseudoglioma syndrome
  • Ovarian overproduction of androgens
  • Pseudohypoaldosteronism type 2
  • Transient neonatal diabetes mellitus
  • Weight control and obesity
more..
Treatments & Procedures
  • Bone densitometry
  • Hormone replacement therapy
  • Dexa scan
  • Insulin treatment
  • Blood glucose monitoring
  • Bone density test
  • Hormone treatments
  • Point of care a1c
  • Dietary counseling
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

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