Marshall Smith Syndrome

Marshall Smith Syndrome

National Organization for Rare Disorders, Inc.

Important

It is possible that the main title of the report Marshall Smith Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.

Synonyms

  • MSS

Disorder Subdivisions

  • None

General Discussion

Marshall-Smith Syndrome is characterized by unusually quick physical growth and bone development (maturation), usually starting before birth. Other symptoms can include respiratory difficulties, mental retardation, and certain physical characteristics. (Note: Marshall-Smith Syndrome is not to be confused with "Marshall" Syndrome, which is very different from "Marshall-Smith" Syndrome.)

Symptoms

In patients with Marshall-Smith Syndrome growth and bone development (maturation) occur faster than normal. The individual is underweight in relation to his or her height and does not thrive well. Other symptoms include diminished muscle tone (hypotonia), muscle weakness, hernias in the abdomen (umbilical hernias), and/or mental retardation. Slow development of voluntary movements (psychomotor retardation) may also occur.



Breathing (respiratory) difficulties commonly occur in patients with Marshall-Smith Syndrome. High-pitched noisy breathing which sounds similar to the wind blowing (stridor), extension of the neck beyond normal limits (hyperextension), or the tongue obstructing the air passage may occur.



Physical characteristics of Marshall-Smith Syndrome include excessive hair growth (hypertrichosis), a long head with a prominent forehead, prominent eyes, and/or an upturned nose with a low nasal bridge. The white of the eye (sclerae) may appear bluish. The angle of the lower jawbone on each side of the face as it joins in the front to form the chin (mandibular ramus) may be smaller than average. Generally, the bones of the fingertips (distal phalanges) are narrow but the rest of the bones in the fingers (proximal and middle phalanges) are broad.



Infrequently, the leaf-shaped structure in the throat which normally prevents food or liquid from passing into the windpipe (epiglottis) may not develop properly in some patients with Marshall-Smith Syndrome. Absent and/or smaller than normal openings leading from the nasal passages into the post-nasal space (choanal atresia and/or stenosis), an abnormal larynx and/or soft cartilage of the larynx (laryngomalacia), a short breastbone (sternum), or a deep crease between the big toe (hallux) and second toe may occur in some patients.



Occasionally, brain abnormalities such as atrophy (cerebral atrophy), larger than normal convolutions of the cerebral cortex (macrogyria), or an absent corpus collosum may occur. (For more information on absence of the corpus collosum, choose "corpus collosum" as your search term in the Rare Disease Database). Defects in the immune system (immunologic defect) are sometimes present. Although rare, some babies with Marshall-Smith Syndrome are born with a sac containing part of the intestines protruding outside the abdominal wall, with the umbilical cord attached (omphalocele).

Causes

The exact cause of Marshall-Smith Syndrome is unknown. There is no evidence that it is genetic.

Affected Populations

Marshall-Smith Syndrome is a rare disorder present at birth affecting males and females in equal numbers. Symptoms of the syndrome are usually present before birth (prenatal onset).

Standard Therapies

Treatment of Marshall-Smith Syndrome is symptomatic and supportive. Aggressive treatment of breathing (respiratory) difficulties is necessary. Special education and related services will be necessary during school years.

Investigational Therapies

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:

www.centerwatch.com

References

TEXTBOOKS

Smith's Recognizable Patterns of Human Malformation, 5th Ed.: Kenneth Lyons Jones, M.D.; W.B. Saunders Co., 1997. Pp. 162-163.



JOURNAL ARTICLES

Marshall-Smith Syndrome: Case Report of a Newborn Male and Review of the Literature. D. A. Summers, et al., Clin Dysmorphol. (Jul 1999, 8 (3)). Pp. 207-10.



Anaesthetic Management of a Child with Marshall-Smith Syndrome. G. Dernedde, et al., Can J Anaesth. (Jul 1998, 45 (7)). Pp. 660-63.



Neonatal Death in Marshall-Smith Syndrome. C. Chatel, et al., Genet Couns. (1998,

9 (1)). Pp. 15-18.



Long Survival of a Patient with Marshall-Smith Syndrome without Respiratory Complications. D. Sperli, et al., J Med Genet. (Oct 1993, 30 (10)).

Pp. 877-79.



Marshall-Smith Syndrome: New Radiograhic, Clinical and Pathological Observations. G. F. Eich et al., Radiology, (Oct 1991, 181 (1)). Pp. 183-188.



FROM THE INTERNET

www.orpha.net/static/GB/marshallsmith_syndrome.html - 48k

Resources

Human Growth Foundation

997 Glen Cove Avenue

Suite 5

Glen Head, NY 11545

Tel: (516)671-4041

Fax: (516)671-4055

Tel: (800)451-6434

Email: hgf1@hgfound.org

Internet: http://www.hgfound.org/



MAGIC Foundation

6645 W. North Avenue

Oak Park, IL 60302

Tel: (708)383-0808

Fax: (708)383-0899

Tel: (800)362-4423

Email: mary@magicfoundation.org

Internet: http://www.magicfoundation.org



Little People of America, Inc.

250 El Camino Real Suite 201

Tustin, CA 92780

Tel: (714)368-3689

Fax: (714)368-3367

Tel: (888)572-2001

Email: info@lpaonline.org

Internet: http://www.lpaonline.org/



Coalition for Heritable Disorders of Connective Tissue (CHDCT)

4301 Connecticut Avenue, NW Suite 404

Washington, DC 20008

Tel: (202)362-9599

Fax: (202)966-8553

Tel: (800)778-7171

Email: chdct@pxe.org

Internet: http://www.chdct2.org/



Genetic and Rare Diseases (GARD) Information Center

PO Box 8126

Gaithersburg, MD 20898-8126

Tel: (301)251-4925

Fax: (301)251-4911

Tel: (888)205-2311

TDD: (888)205-3223

Internet: http://rarediseases.info.nih.gov/GARD/



MSS Research Foundation (Marshall-Smith Syndrome)

Oeverbiesstraat 20

The Hague, NL 2548 WP

The Netherlands

Tel: 31703356956

Email: info@marshallsmith.org

Internet: http://www.marshallsmith.org



For a Complete Report

This is an abstract of a report from the National Organization for Rare Disorders, Inc.® (NORD). Cigna members can access the complete report by logging into myCigna.com. For non-Cigna members, a copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html.

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