Female Hair Loss Laboratory Panel
About
The Female Hair Loss Laboratory Panel is a blood testing package that measures selected sex and thyroid hormones that may be relevant when evaluating hair thinning or increased hair shedding in women. The panel includes free testosterone, total testosterone, DHEA-S, estrogen, follicle-stimulating hormone (FSH), luteinizing hormone (LH), progesterone, thyroid-stimulating hormone (TSH), free triiodothyronine (fT3), and free thyroxine (fT4).
These results can help identify hormonal or thyroid-related findings that may contribute to hair loss. The panel evaluates only one part of the possible causes. A scalp examination, the pattern and speed of hair loss, current medications, recent stress, nutrition, menstrual history, pregnancy, menopause, and previous illnesses are also important when deciding what further assessment may be needed.
What the panel measures
- Androgen-related markers: free testosterone, total testosterone, and DHEA-S can support evaluation of androgen activity when hair loss occurs with signs such as acne, increased facial or body hair, or menstrual irregularity.
- Reproductive hormones: estrogen, FSH, LH, and progesterone provide information that must be interpreted in relation to age, menstrual cycle phase, pregnancy, perimenopause, menopause, and the use of hormonal contraception or hormone therapy.
- Thyroid hormones: TSH, fT3, and fT4 help assess thyroid function, which may be relevant when hair changes occur together with symptoms such as fatigue and low energy or weight gain and difficulty losing weight.
When this laboratory panel may be considered
The panel may be considered when a woman notices persistent shedding, reduced hair density, widening of the central part, diffuse thinning across the scalp, or changes that occur alongside menstrual, thyroid, or other hormone-related symptoms. It may also be useful as part of a broader assessment in perimenopause or menopause, or when hormonal medication could influence the clinical picture.
Female pattern hair loss and other common forms of hair loss can occur even when hormone levels are within the laboratory reference range. The results therefore cannot confirm or exclude every possible cause and should not be interpreted as a diagnosis on their own.
What the panel does not assess
This package does not provide a complete assessment of nutritional, hematologic, autoimmune, inflammatory, infectious, genetic, or medication-related causes of hair loss. Depending on the symptoms and medical history, a doctor may consider additional tests such as a complete blood count, iron and ferritin testing, or other selected laboratory investigations. These tests are separate from this panel.
A clinical scalp examination remains important. The distribution of thinning, the presence of broken hairs, scaling, redness, pain, pustules, smooth patches, scarring, or loss of eyebrows and eyelashes can change the diagnostic pathway. Dermoscopy or trichoscopy may also be considered during a dermatology evaluation.
Preparation and timing
A venous blood sample is required. Before the appointment, confirm whether fasting is needed and whether testing should be coordinated with a particular phase of the menstrual cycle. Hormone concentrations can vary during the cycle, and interpretation may differ for women who are pregnant, perimenopausal, postmenopausal, or using hormonal contraception or hormone replacement therapy.
Prepare the date of the last menstrual period and the current cycle day when applicable. Report all prescription medications, hormonal products, over-the-counter medicines, and supplements. Do not stop prescribed medication or supplements solely for this test unless instructed by a qualified healthcare professional.
How testing is performed
Step 1: Review of relevant information
Information about the hair loss pattern, menstrual cycle, pregnancy or menopause status, medications, supplements, and previous laboratory findings helps place the results in context.
Step 2: Venous blood collection
A blood sample is collected from a vein, usually in the arm. The collection itself generally takes only a few minutes.
Step 3: Laboratory analysis
The sample is analyzed for the ten markers included in the panel: free testosterone, total testosterone, DHEA-S, estrogen, FSH, LH, progesterone, TSH, fT3, and fT4.
Step 4: Interpretation and possible next steps
The report presents the measured values and applicable laboratory reference intervals. Interpretation should account for age, menstrual cycle timing, menopausal status, pregnancy, symptoms, medications, and hormone therapy. A single result outside the reference interval does not establish the cause of hair loss, while results within range do not exclude non-hormonal causes.
When further evaluation may be needed
A dermatology assessment is particularly important when hair loss is sudden, rapidly progressive, patchy, painful, associated with scalp inflammation, or accompanied by visible scarring. Depending on the findings, further evaluation may include additional blood tests or consultation in dermatology, gynecology, or endocrinology.
Before sending an inquiry, prepare information about when the hair loss began, whether it is diffuse or localized, how quickly it is progressing, menstrual changes, pregnancy or menopause status, recent illness, significant stress, diet, medications, supplements, and any previous laboratory reports. Clear photographs of the scalp or hair part may also help describe the pattern. You can send this information through ZagrebMed to request laboratory testing and clarify the most appropriate next step.
Candidate
The panel may be considered for women with persistent increased shedding, diffuse thinning, reduced hair density, or a widening hair part, particularly when hair changes occur with menstrual irregularity, acne, increased facial or body hair, menopausal symptoms, fatigue, weight changes, or other possible hormonal or thyroid-related concerns. It is not a complete hair loss assessment and does not replace a scalp examination. Sudden, patchy, inflamed, painful, or scarring hair loss should be evaluated clinically rather than assessed through laboratory testing alone.
Preparation
Confirm before testing whether fasting is required and whether blood collection should be scheduled during a particular phase of the menstrual cycle. When applicable, note the first day of the last menstrual period and the current cycle day. Report pregnancy, perimenopause, menopause, hormonal contraception, hormone therapy, prescription medications, and supplements. Do not stop medication or supplements unless a qualified healthcare professional specifically advises you to do so.
Treatment
The service involves collection of one venous blood sample, usually from the arm. The sample is analyzed for free testosterone, total testosterone, DHEA-S, estrogen, FSH, LH, progesterone, TSH, fT3, and fT4. Blood collection usually takes only a few minutes, after which normal daily activities can generally be resumed.
Result
The laboratory report provides the individual hormone values and applicable reference intervals. Results should be interpreted in relation to age, menstrual cycle phase, pregnancy or menopausal status, symptoms, medications, and hormone therapy. Abnormal findings may support further assessment, but they do not identify the cause of hair loss by themselves. Normal results do not exclude female pattern hair loss, stress-related shedding, nutritional deficiencies, scalp disorders, medication effects, or other non-hormonal causes.
Precautions
Temporary discomfort, minor bruising, or lightheadedness can occur after blood collection. Inform the person collecting the sample if you have a history of fainting, difficult blood draws, bleeding disorders, or use medication that affects clotting. Do not start hormonal treatment or high-dose supplements based only on laboratory values. Sudden patchy hair loss, scalp redness, scaling, pain, pustules, scarring, or loss of eyebrows or eyelashes warrants timely clinical evaluation.

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