The 20 Best Neu Laxova Syndrome Doctors Near Me in davis, CA

Find the Top Neu Laxova Syndrome Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 2 doctor with experience in Neu Laxova Syndrome near davis, CA. Of these, 2 are Experienced.

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2 providers found
    Experienced in Neu Laxova Syndrome
    Family Medicine
    Experienced in Neu Laxova Syndrome
    Family Medicine

    The Center For Community Health & Well Being Inc

    1900 T St, 
    Sacramento, CA 
     (13.8 miles away)
    Languages Spoken:
    English, Vietnamese
    Accepting New Patients

    Madeline Nguyen is a primary care provider, practicing in Family Medicine in Sacramento, California. Dr. Nguyen is rated as an Experienced provider by MediFind in the treatment of Neu Laxova Syndrome. She is also highly rated in 49 other conditions, according to our data. Her clinical expertise encompasses Type 2 Diabetes (T2D), Maturity Onset Diabetes of the Young, Sciatica, and Glucocorticoid-Remediable Aldosteronism. Dr. Nguyen is currently accepting new patients.

    Experienced in Neu Laxova Syndrome
    Family Medicine
    Experienced in Neu Laxova Syndrome
    Family Medicine

    Office

    3160 Folsom Blvd Ste 2500, 
    Sacramento, CA 
     (14.9 miles away)
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Jacob Dima is a primary care provider, practicing in Family Medicine in Sacramento, California. Dr. Dima is rated as an Experienced provider by MediFind in the treatment of Neu Laxova Syndrome. He is also highly rated in 18 other conditions, according to our data. His clinical expertise encompasses Hypothyroidism, Vitamin D Deficiency, High Cholesterol, and Autosomal Recessive Hypotrichosis. Dr. Dima is currently accepting new patients.

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    Last Updated: 09/26/2026

    What is the definition of Neu Laxova Syndrome?

    Neu Laxova syndrome (NLS) is a genetic disorder affecting many parts of the body. Babies born with NLS usually grow poorly during pregnancy (intrauterine growth restriction). At birth, they may be small (low birth weight and short in length) and their facial features are usually different and distinct. The babies may have a small head (microcephaly), sloping forehead, and widely spaced eyes (hypertelorism). Babies with NLS may also have extra fluid (edema) in their hands and feet, brain abnormalities, and rigid, stiff muscles. Other birth defects may affect the baby's arms, legs, skin, genitals, kidneys, and heart. Not every baby with NLS will have every sign or symptom of NLS. Neu Laxova syndrome (NLS) is caused by changess in one of three different genes, PHGDH, PSAT1, PSPH. The genetic changes cause too little L-serine (an amino acid) to be made. There must be a genetic change in both copies of one of these genes, which means NLS is inherited in an autosomal recessive manner. NLS can be diagnosed both prenatally by an ultrasound or after birth. The diagnosis is suspected by signs and symptoms, but may be confirmed by genetic testing (prenatally by chorionic villi sampling (CVS) or amniocentesis; after birth by genetic blood test).