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

Find the Top Neu Laxova Syndrome Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 3 doctor with experience in Neu Laxova Syndrome near pomona, CA. Of these, 3 are Experienced.

Location
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3 providers found
    Experienced in Neu Laxova Syndrome
    Medical Genetics | Pediatrics
    Experienced in Neu Laxova Syndrome
    Medical Genetics | Pediatrics
    Referral may be required

    Faculty Physicians And Surgeons Of Llusm

    901 San Bernardino Rd, Suite 104and302, 
    Upland, CA 
     (7.1 miles away)
    Languages Spoken:
    English

    Hua Wang is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Upland, California. Dr. Wang is rated as an Experienced provider by MediFind in the treatment of Neu Laxova Syndrome. Her clinical expertise encompasses Miller-Dieker Syndrome, Smith-Magenis Syndrome, Hypochondroplasia, and Achondroplasia.

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

    9190 Haven Ave

    9190 Haven Ave Ste 102, 
    Rancho Cucamonga, CA 
     (10.3 miles away)
    Languages Spoken:
    English
    Accepting New Patients

    Ani Berberyan is a primary care provider, practicing in Family Medicine in Rancho Cucamonga, California. Dr. Berberyan is rated as an Experienced provider by MediFind in the treatment of Neu Laxova Syndrome. She is also highly rated in 11 other conditions, according to our data. Her clinical expertise encompasses Obesity, Axillary Nerve Dysfunction, Sciatica, and High Cholesterol. Dr. Berberyan is currently accepting new patients.

    Experienced in Neu Laxova Syndrome
    Medical Genetics | Oncology
    Experienced in Neu Laxova Syndrome
    Medical Genetics | Oncology
    Referral may be required

    City Of Hope Medical Foundation

    1500 Duarte Rd, 
    Duarte, CA 
     (13.7 miles away)
    Languages Spoken:
    English

    Stephen Gruber is a Medical Genetics specialist and an Oncologist practicing medicine in Duarte, California. Dr. Gruber is rated as an Experienced provider by MediFind in the treatment of Neu Laxova Syndrome. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Colorectal Cancer, Familial Colorectal Cancer, Lynch Syndrome, Melanoma, and Colonoscopy.

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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).