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Wiedemann Rautenstrauch Syndrome


Última actualización: June 01, 2016
Años publicados: 1997, 2001, 2003, 2010, 2016


NORD gratefully acknowledges Eniko Karman Pivnick, MD, professor at the University of Tennessee Health Science Center, for assistance in the preparation of this report.


Wiedemann-Rautenstrauch syndrome (WRS), also known as neonatal progeroid syndrome, is a very rare genetic disorder characterized by an aged appearance at birth (old man look) growth delays before and after birth (prenatal and postnatal growth retardation), and deficiency or absence of the layer of fat under the skin (subcutaneous lipoatrophy). It is anticipated that most individuals with WRS have decreased life expectancy. There are few individuals who have lived well in to their teens and even fewer still alive in their 20s. WRS represents a complex of symptoms and signs with an unknown cause, and pathogenesis remains distinct enough to allow a secure diagnosis. WRS is inherited as an autosomal recessive trait, as several pairs of siblings have been reported in families with unaffected parents. Few of the parents were related by blood (consanguineous).

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  • neonatal progeroid syndrome
  • neonatal pseudo-hydrocephalic progeroid syndrome of WRS
  • Rautenstrauch-Wiedemann syndrome
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Signos y Síntomas

WRS is characterized by an aged appearance at birth and deficiency or absence of the layer of fat under the skin (subcutaneous lipoatrophy). As a result, the skin may appear unusually thin, fragile, dry, shiny, wrinkled, and aged. Certain veins and muscles may be abnormally prominent, particularly those of the forehead. For unknown reasons, as affected infants age, abnormal deposits of fat may accumulate under the skin (subcutaneous) in lower (caudal) areas of the body, particularly around the buttocks, the areas around the genitals and the anus (anogenital area), and the area between the ribs and the hips (flanks). In addition, in infants and children with the disorder, the abdomen may appear unusually large and prominent.

In individuals with WRS, growth delays may occur before birth (intrauterine growth retardation), particularly during the last three months (third trimester) of fetal development. The growth delays will continue well after birth (postnatal). Patients with WRS also experience poor weight gain, and failure to thrive through their lifetime. In addition, in some cases, affected infants may experience swallowing (dysphagia) and feeding difficulties that may contribute to growth delays and failure to thrive.

Progressive neurological deterioration may occur in WRS. The specific symptoms may vary from person to person as affected individuals may not have all of the symptoms listed below.

Infants and children with WRS also have distinctive abnormalities of the head and face (craniofacial). In many affected individuals, the soft spot in the front of the skull (anterior) may be abnormally large and wide, and its closure may be unusually delayed. The fibrous gaps between other bones in the skull (cranial sutures) may also be abnormally wide. In addition, in infants with the disorder, bones of the forehead (frontal bones) and the sides of the skull (parietal bones) are abnormally prominent (frontal and bi-parietal bossing), while the facial bones are unusually small and underdeveloped (hypoplastic).

Such abnormalities may cause the head to appear unusually large (pseudohydrocephalus). In affected infants and children, distinctive facial abnormalities may include an unusually small mouth (microstomia); a prominent chin, and low-set ears that are abnormally angled toward the back of the head (posteriorly angulated). Facial features typically appear unusually small when compared with the large forehead and sides of the skull. In addition, affected infants may have an unusually small, distinctively “beak-shaped” nose that becomes more pronounced with advancing age.

In most infants and children with WRS, additional craniofacial abnormalities are also present. Affected infants may have two to four front teeth (neonatal incisors), which fall out during the course of early infancy. Subsequent tooth development (dentition) is delayed and impaired. In addition, in infants and children with the disorder, the lower eyelids may droop or turn outward (ectropion), exposing the thin, delicate mucous membranes that line the eyelids as well as a portion of the eyeballs (conjunctivae). In one patient, spastic entropion, a condition in which the eyelid turns inward so that the eyelashes and skin rub against the eye surface, was also described. An interesting feature in a few cases is that the lower eyelids may cover more than the lower half of the eyeball as if the eyelids are situated higher than expected. Affected infants and children may also have unusually sparse scalp hair, eyebrows, and eyelashes. (hypotrichosis). In a family with three affected siblings, various eye abnormalities including cataract, cloudy cornea, perforation of cornea, and microphthalmia (unusually small size of the eye) also were noted.

Infants and children with WRS may also have distinctive abnormalities affecting the hands, feet, arms, and legs (extremities). The arms and legs are abnormally thin, the hands and feet are disproportionately large; and the fingers and toes are long with unusually small, incompletely developed (atrophic) or thickened (dystrophic) nails. The joints are thick and rigid, especially in the shoulders, elbows and knees. Recent MRI (magnetic resonance imaging) studies have confirmed the presence of normal amounts of subcutaneous truncal fat, and marked loss of fat from the face and distal extremities. Bone thinning (osteopenia) may predispose to bony fractures. Bone progenitor cell transformation to bone (osteoblasts) and cartilage cells (chondrocytes) are also impaired. The lack of cellular differentiation capacity in WRS patients may be responsible for the clinical appearance and symptoms of this rare disorder.

Most infants and children with the disorder also have varying degrees of intellectual disability, which may range from mild to severe. However, a few children have demonstrated near normal mental development. During infancy, affected individuals may begin to experience progressive neurological and neuromuscular abnormalities. In most patients, there are severe delays in the acquisition of skills requiring the coordination of physical and mental activities (psychomotor retardation). In addition, in many cases, infants and children with the disorder lack head control, exhibit diminished muscle tone (hypotonia), and have an impaired ability to coordinate voluntary movements of the chest and abdominal areas (truncal ataxia). For example, they may have difficulty controlling the range of movements during certain muscular actions and may experience rhythmic, involuntary tremors when performing certain movements (intention tremor). Infants and children with the disorder may also experience rapid, involuntary, horizontal movements of the eyes (horizontal nystagmus) and limited clearness (acuity) of vision. Infants may have dysphonic, horse cry and older children may have an unusual high-pitched voice.

In addition, investigators have reported that neurological deterioration observed in a few individuals with WRS may be associated with loss of the myelin sheath from nerve fibers (demyelization) within the white substance of the brain (e.g., pure sudanophilic leukodystrophy). Myelin is a whitish fatty substance that forms a protective wrapping or “sheath” around certain nerve fibers (axons) and serves as an electrical insulator, enabling the effective transmission of nerve impulses. “White substance” within the brain and spinal cord (central nervous system) primarily consists of bundles of myelinated nerve fibers. The majority of patients with WRS did not have leukodystrophy at the age ascertained. Dandy Walker malformation and ventriculomegaly, basal ganglia calcification, and agenesis of corpus callosum were reported.

The lack of subcutaneous fat tissue has prompted researchers to compare WRS with generalized lipodystrophy (Berardinelli) syndrome. Laboratory studies, however, in those cases examined, have shown no elevation of fasting glucose, lipids, or insulin, as would be expected in Berardinelli syndrome. A few patients however, had elevated triglyceride levels. Fat pads are localized at the flank, rather than at the buttocks, which is specific for this syndrome, but also can be seen in carbohydrate deficient glycoprotein syndrome (CDG). Individuals with WRS may also develop abnormal side-to-side curvature of the spine (scoliosis). In addition, infants and children with WRS are often prone to recurrent respiratory infections, which may result in life-threatening complications.

In one of the few cases where post mortem pathology was performed, an almost total absence of the mesentery, a tissue that anchors the small intestines to the back of the abdominal wall, and absence of the mesocolon, the tissue that secures the transverse portion of the large intestines, were found.

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Causas y Herencia

WRS is most likely inherited as an autosomal recessive genetic condition. Several siblings with WRS have been reported in unrelated families.

Recessive genetic disorders occur when an individual inherits two copies of an abnormal gene for the same trait, one from each parent. If an individual receives one normal gene and one gene for the disease, the person is a carrier for the disease but usually will not show symptoms. The risk for two carrier parents to have an affected child is 25% with each pregnancy. The risk to have a child who is a carrier like the parents is 50% with each pregnancy. The chance for a child to receive normal genes from both parents is 25%. The risk is the same for males and females.

Some individuals with WRS have had parents, who were related by blood (consanguineous).

All individuals carry several abnormal genes. Parents who are close relatives (consanguineous) have a higher chance than non-consanguineous parents to carry the same abnormal gene, which increases the risk to have children with a rare recessive genetic disorder.

The specific underlying defect responsible for the disorder remains unknown. However, some researchers suggest that disturbances in bone maturation and hormonal and fatty (lipid) metabolism may play some role.

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WRS is an extremely rare genetic disorder that appears to affect males and females relatively equally. WRS has been observed in various ethnic and racial groups. The disorder was initially described as a distinct entity in 1979 (Wiedemann HR) based upon observation of two unrelated individuals as well as previous reports of two affected sisters in 1977 (Rautenstrauch T). More than 35 affected individuals have been reported in the medical literature to date.

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In some cases, growth disability, macrocephaly, and/or other characteristic findings suggestive of Wiedemann-Rautenstrauch Syndrome may be detected before birth (prenatally) by ultrasound.

In most patients, Wiedemann-Rautenstrauch syndrome is diagnosed shortly after birth, based upon a thorough clinical evaluation and identification of characteristic physical findings (e.g., short stature, characteristic craniofacial and skeletal malformations, absence or deficiency of subcutaneous fat, etc.). In some cases, specialized tests may also be conducted to detect certain abnormalities potentially associated with the disorder. For example, X-ray studies may reveal and/or confirm wide cranial sutures and/or other abnormalities of cranial bones. In addition, it is possible that computer-assisted tomography (CAT), magnetic resonance imaging (MRI), and/or other specialized tests may reveal widespread loss of the fatty coverings (myelin sheath) on nerve fibers (demyelination) within the white matter of the brain (pure sudanophilic leukodystrophy) or other abnormalities as described above.

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The treatment of Wiedemann-Rautenstrauch syndrome is directed toward the specific symptoms that are apparent in each individual. Treatment may require the coordinated efforts of a team of specialists. Pediatricians, specialists who assess and treat disorders of the nervous system (neurologists), physical therapists, and/or other health care professionals may need to systematically and comprehensively plan an affected child’s treatment.

Specific therapies for Wiedemann-Rautenstrauch syndrome are symptomatic and supportive. In some cases, if affected infants and children experience swallowing and feeding difficulties and cannot feed appropriately by mouth, a tube may be surgically inserted into the stomach or a portion of the small intestine (tube feeding) to help provide appropriate nourishment. In addition, affected infants and children should be carefully monitored to help guard against respiratory infections. Genetic counseling will be of benefit for affected individuals and their families.

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Information on current clinical trials is posted on the Internet at www.clinicaltrials.gov. All studies receiving U.S. government funding, and some supported by private industry, are posted on this government web site.

For information about clinical trials being conducted at the NIH Clinical Center in Bethesda, MD, contact the NIH Patient Recruitment Office:
Tollfree: (800) 411-1222
TTY: (866) 411-1010
Email: prpl@cc.nih.gov

For information about clinical trials sponsored by private sources, contact:

For information about clinical trials conducted in Europe, contact:

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(Please note that some of these organizations may provide information concerning certain conditions potentially associated with this disorder [progeroid appearance, neurological abnormalities, intellectual disability, etc.].)

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Pivnick EK. Neonatal Progeroid Syndrome. In: NORD Guide to Rare Disorders. Lippincott Williams & Wilkins. Philadelphia, PA. 2003:238-39.

Champion RH, et al., eds. Textbook of Dermatology. 5th ed. Cambridge, MA: Blackwell Scientific Publications, Inc.; 1992:1817.

Gorlin RJ, et al., eds. Syndromes of the Head and Neck. 3rd ed. New York, NY: Oxford University Press; 1990:488.

Buyse ML. Birth Defects Encyclopedia. Dover, MA: Blackwell Scientific Publications, Inc.; 1990:420-22, 476, 1278-79, 1411-14.


Rabah M Shawky et al.: Neonatal Progeroid Syndrome (Wiedemann Rautentrauch Syndrome in an Egyptian Child with premature loss of teeth and café au lait skin patches. The Egyptian Journal of Medical Human Genetics. 2012;13;227-231

Arboleda G,et al.: Neonatal Progeroid Syndrome (Widemann-Rautenstrauch Syndrome) Report of Three Affected Sibs. Am J Med Genet A. 2010;155:1712-1715

Hou JW. Natural course of neonatal progeroid syndrome. Pediatr Neonatol 2009;50(3):102–9.

Arboleda G, Ramirez N, Arboleda H. The neonatal progeroid syndrome (Wiedemann-Rautenstrauch): a model for the study of human aging? Exp Gerontol. 2007 Oct; 42(10):939-43. Epub 2007 Jul 19.

O’Neill B, et al.:Body fat distribution and metabolic variables in patients with neonatal progeroid syndrome.. AmJ Med Genet A 2007 July 1;143A(13):1421-30

O’Neill B, Simha V, Kotha V, Garg A.: Body fat distribution and metabolic variables in patients with neonatal progeroid syndrome. Am J Med Genet A. 2007 Jul 1;143 (13):1421-30.

Jäger M et al.: In vitro osteogenic differentiation is affected in Wiedemann-Rautenstrauch-Syndrome (WRS). In Vivo.2005 Sept-Oct;19(5):831-6.

Arboleda H and Arboleda G.: Follow-up study of Wiedemann-Rautenstrauch syndrome: long term survival and comparison with Rautenstrauch’s patient “G”. Birth Defects Res A Clin Mol Teratol. 2005 Aug;73(8):562-8.

Hoppen T et al.: Siblings with neonatal progeroid syndrome (Wiedemann-Rautenstauch). Klin Padiatr. 2004 Mar-Apr;216(2):70-1.

Cao H and Hegele RA.: LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedeman-Rautenstrauch progeroid syndrome (MIM 264090). J Hum Genet. 2003; Vol 48,Number 5,271-274.

Thorey F, et al.: Kyphoscoliosis in Wiedemann-Rautenstrauch syndrome (neonatal progeroid syndrome). Z Orthop Ihre Grenzgeb. 2003;141:341-4.

Korniszewski L, et al.: Wiedemann-Rautenstrauch (neonatal progeroid) syndrome: new case with normal telomere length in skin fibroblasts. Am J Med Genet. 2001;103:144-8.

Korniszewski L et al. Wiedemann-Rautenstrauch (neonatal progeria) syndrome: New case with normal telomere length in skin fibroblasts. Am J Med Genet. 2001: October 1;103(2): 144-148.

Pivnick EK, et al.: Neonatal progeroid (Wiedemann-Rautenstrauch) syndrome: report of five new cases and review. Am J Med Genet. 2000;90:131-40.

Hoppen T, et al.: Neonatal progeroid syndrome (Wiedemann-Rautenstrauch syndrome): case report and review of the literature. Klin Padiatr. 2000;212:71-76.

Abdel-Salam GM, Czeizel AE. A new case of neonatal progeroid syndrome with agenesis of corpus callosum. Genet Couns 1999;10(4):377–81.

Stoll C, et al.: Wiedemann-Rautenstrauch syndrome. A case report and review of the literature. Genet Couns. 1998;9:119-24.

Courtens W, et al.: A probable case of Wiedemann-Rautenstrauch syndrome or neonatal progeroid syndrome and review of the literature. Clin Dysmorphol. 1997;6:219-27.

Arboleda H, et al.: Wiedemann-Rautenstrauch neonatal progeroid syndrome: report of three new patients. J Med Genet. 1997;34:433-37.

Bitoun P, et al.: The Wiedemann-Rautenstrauch neonatal progeroid syndrome: a case report and review of the literature. Clin Dysmorphol. 1995;4:239-45.

Rautenstrauch T, et al.: Neonatal progeroid syndrome (Wiedemann-Rautenstrauch). A follow-up study. Klin Padiatr. 1994;206:440-43.

Mazzarello P, et al.: Enzymes of DNA metabolism in a patient with the Wiedemann-Rautenstrauch progeroid syndrome. Ann N Y Acad Sci. 1992;663:440-41.

Castineyra G, et al.: Two sibs with Wiedemann-Rautenstrauch syndrome: possibilities of prenatal diagnosis by ultrasound. J Med Genet. 1992;29:434-36.

Toriello HV.: Wiedemann-Rautenstrauch syndrome. J Med Genet. 1990;27:256-57.

Hagadorn JI, et al.: Neonatal progeroid syndrome: more than one disease? Am J Med Genet. 1990;35:91-94.

Rudin C, et al.: The neonatal pseudo-hydrocephalic progeroid syndrome (Wiedemann-Rautenstrauch). Report of a new patient and review of the literature. Eur J Pediatr. 1988;147:433-38.

Martin JJ, et al.:The Wiedemann-Rautenstrauch or neonatal progeroid syndrome. neuropathological study of a case. Neuropediatrics. 1984;15:43-48.

Devos EA, et al.: The Wiedemann-Rautenstrauch or neonatal progeroid syndrome. Report of a patient with consanguineous parents. Eur J Pediatr. 1981;136:245-48.

Wiedemann HR.: An unidentified neonatal progeroid syndrome: follow-up report. Eur J Pediatr. 1979;130:65-70.

Rautenstrauch T, et al.: Progeria: a cell culture study and clinical report of familial incidence. Eur J Pediatr. 1977;124:101-11.

Gordon LB, Brown WT, Collins FS. Hutchinson-Gilford Progeria Syndrome. 2003 Dec 12 [Updated 2015 Jan 8]. In: Pagon RA, Adam MP, Ardinger HH, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1121/ Accessed June 1, 2016.

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