Neonatal Progeroid Syndrome: Causes, Symptoms, And Treatment

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Neonatal progeroid syndrome or Wiedemann-Rautenstrauch syndrome is a type of progeria (a rare, progressive genetic disorder) characterized by an aged appearance at birth, sparse hair, developmental delay before and after birth, and fat loss under the skin.

It is believed that neonatal progeroid syndrome is inherited in an autosomal recessive manner and affects around one in four million newborns worldwide (1). Most children with this condition have a life span of a few months; however, in some cases, they live into their teens and 20s (2) (3).

Read on to learn more about the signs and symptoms of neonatal progeroid syndrome, its causes, diagnosis, and possible treatment options.

Signs And Symptoms Of Neonatal Progeroid Syndrome

Neonatal progeroid syndrome presents itself through several complex signs and symptoms, which could vary among babies with the condition. The signs could be visible before birth during prenatal ultrasounds and could be confirmed at birth. In most cases, parents may spot changes in the baby’s physical appearance, or the doctor may notice them during routine checkups.

The signs and symptoms of the neonatal progeroid syndrome in babies include (3) (4):

  • Growth delays of the baby inside the mother’s womb (intrauterine growth retardation)
  • Deficiency or absence of fat layer under the skin, giving the baby an aged appearance
  • Dry, thin, wrinkled, and shiny skin
  • Unusually prominent veins on the forehead
  • Unusually large and prominent abdomen
  • Facial features characterized by a triangular face, large skull with a prominent forehead, beaked nose, small mouth with thin upper lip, and low-set ears angled towards the back of the head (craniofacial abnormalities)
  • The lower eyelid turned outwards, exposing a part of the eyeball
  • Sparse hair on scalp, eyebrows, and eyelashes
  • Thin and disproportionately large arms and legs
  • Long fingers and toes with incompletely developed nails
  • Larger than normal soft spot (the space between the skull bones), which stays open throughout life
  • A few infants are born with teeth (natal teeth) that fall after a few weeks of birth
  • Delayed or impaired development of permanent teeth
  • Difficulty with coordination and balance

These signs may also occur in other problems, such as birth defects, in babies. Therefore, seek doctor consultation as soon as you notice them.

Complications Of Neonatal Progeroid Syndrome

Apart from the symptoms discussed, some infants with neonatal progeroid syndrome develop other complications, too (3).

  • Difficulty in feeding and swallowing
  • Possibility of developing scoliosis (unusual sideways curve in the spine)
  • Abnormalities in bone maturation
  • Low bone density that might lead to fracture
  • Repeated respiratory complications
  • Absence of mesentery, a membrane that attaches the small intestine to the abdominal wall
  • Intellectual disability, ranging from mild to severe
  • Neurological deterioration due to the loss of myelin sheath from nerve fibers in the white substance of the brain (demyelination)

Causes Of Neonatal Progeroid Syndrome

Neonatal progeroid syndrome is believed to be an autosomal recessive genetic disorder. The baby inherits one copy of a mutated gene (an altered gene that forms faulty proteins) for the same trait from each parent.

The progeroid syndrome occurs when there is a mutation in the gene called POLR3A. This gene makes the subunit (the largest piece) of an enzyme called RNA polymerase III. This enzyme helps synthesize several types of RNA, which, in turn, assemble amino acids into proteins.

Due to the defective POLR3A gene, the assembly of amino acids is affected, and abnormal proteins are made. These proteins may hamper an individual’s normal development and function, but how the symptoms are exactly expressed remains unknown (5).

Risk Factors For Neonatal Progeroid Syndrome

The symptoms of a recessive genetic disorder, such as neonatal progeroid syndrome, are only expressed when the child receives a defective gene copy from each parent. If the child receives one mutated gene and a healthy one, the child will not show symptoms but will become a carrier.

If both the parents are carriers, the risk of having an affected child is 25%, a carrier child is 50%, and a child with normal genes is 25% with each pregnancy. Parents related by blood have a higher chance of having children with genetic disorders because they might carry the same mutated genes (2).

Diagnosis Of Neonatal Progeroid Syndrome

Sometimes, an ultrasound can diagnose neonatal progeroid syndrome before birth (prenatal diagnosis) by identifying characteristics, such as growth disability or unusually large head.

However, in most cases, the healthcare providers detect progeroid syndrome during regular checkups after the birth of the child. The characteristic symptoms, such as deficiency of fat layer, a prominent head, and unusual facial features, help identify the disease.

Other specific tests are also conducted to identify the problems associated with neonatal progeroid syndrome. These are:

  • X-ray: It helps detect deformity in the cranial bones.
  • Computer-assisted tomography or magnetic resonance imaging: It helps detect neurological abnormalities or other malformations (2).

Treatment For Neonatal Progeroid Syndrome

There is no specific cure for neonatal progeroid syndrome since it is a genetic condition. Treatment options are primarily supportive, reducing the intensity of the symptoms and improving the child’s life quality, especially as they grow older.

The treatment of neonatal progeroid syndrome is symptom-based and differs from one child to another. In most cases, the best approach is discussed by a team of doctors, including neurologists and physical therapists. The primary focus could be to ensure the baby gets adequate nourishment. Therefore, feeding tubes could be utilized in many cases. As the baby grows older, different types of therapies could be suggested to help the child have minimal limitations due to the syndrome (6).

Frequently Asked Questions

1. At what age is progeria diagnosed?

The symptoms of progeria may not show at birth and may take around 18 to 24 months to become evident (7).

2. Can progeria be prevented?

To date, no scientifically proven preventive methods exist for progeria.

3. Can I test for progeria while pregnant?

Progeria is a rare genetic disorder caused by a mutation in the LMNA gene (called “lamin-A”). Hence, progeria testing is not included in routine prenatal tests. Your doctor may suggest additional tests to look for the LMNA genetic change responsible for progeria in the fetus (8).

The symptoms of neonatal progeroid syndrome start developing soon after birth, so you must see a doctor if you find any unusual changes in your child. It is important to seek help from specialists, create a supportive environment at home, and include the baby in as many activities as possible. Talking out your concerns during a professional counseling session may also help manage the condition better.

Key Pointers

  • Prenatal ultrasound scans may show symptoms of the neonatal progeroid syndrome, which can be confirmed once the baby is born.
  • It’s an autosomal recessive genetic condition caused by a POLR3A gene mutation.
  • Treatment is based on the symptoms and specific to each baby, with the primary goal of providing appropriate nutrition to the newborn.


MomJunction's articles are written after analyzing the research works of expert authors and institutions. Our references consist of resources established by authorities in their respective fields. You can learn more about the authenticity of the information we present in our editorial policy.
  1. About Progeria.
  2. Autosomal recessive.
  3. Wiedemann Rautenstrauch Syndrome.
  4. Rabah M.Shawky et al. (2012); Neonatal progeroid syndrome (Wiedemann-Rautenstrauch syndrome) in an Egyptian child with premature loss of teeth and café au lait skin patches.
  5. Wiedemann-Rautenstrauch syndrome.
  6. Neonatal progeroid syndrome.
  7. Progeria: Hutchinson-Gilford Progeria Syndrome (HGPS).
  8. Progeria 101 / FAQ.
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Pragya Bhargavi

Pragya Bhargavi has been in the field of content research, writing and editing for over five years. Her passion for academics and science has enabled her to write creative as well as research-based articles. She has completed her Masters in Microbiology from Bangalore University and obtained a Bachelor’s degree in Education (B.Ed) from Acharya Nagarjuna University, Guntur. As a writer at... more

Dr. Dur Afshar Agha

Dr. Dur Afshar Agha is a consultant pediatrician with decades of experience in various medical facilities both in Pakistan and Saudi Arabia. She has headed the Department of Preventive Pediatrics at the prestigious, Children’s Hospital and Institute of Child Health in Pakistan and is a life member of the Pakistan Paediatric Association. She has also completed her Post Graduate Program... more