marshall smith syndrome

Marshall-Smith syndrome | Genetic and Rare Diseases

80 rows · Jun 14, 2017 · Summary Summary. Marshall-Smith syndrome (MRSHSS) is a genetic disorder in which individuals typically have advanced bone age, difficulties gaining weight (failure to thrive), unique facial features, and intellectual disability. Other signs and symptoms of this condition may include eye abnormalities, breathing difficulties, and neurological issues.

MEDICAL TERMS OTHER NAMES LEARN MORE: HPO ID
Accelerated skeletal maturation Advanced bone age Early bone maturation … 0005616
Anteverted nares Nasal tip, upturned Upturned nasal tip Uptu… 0000463
Bowing of the long bones Bowed long bones Bowing of long bones [ … 0006487
Failure to thrive Faltering weight Weight faltering [ more ] 0001508

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Marshall Smith Syndrome – NORD (National Organization for

Related Disorders. Weaver Syndrome is similar to Marshall-Smith Syndrome in that growth and bone maturation occur faster than normal. However, patients with Weaver Syndrome have normal to above normal weight in relation to their height whereas patients with Marshall-Smith Syndrome are underweight in relation to their height.

Marshall–Smith syndrome – Wikipedia

Overview

OMIM Entry – # 602535 – MARSHALL-SMITH SYNDROME; MRSHSS

▼ Description. The Marshall-Smith syndrome is a malformation syndrome characterized by accelerated skeletal maturation, relative failure to thrive, respiratory difficulties, mental retardation, and unusual facies, including prominent forehead, shallow orbits, blue sclerae, depressed nasal bridge, and micrognathia ( Adam et al., 2005 ).

Marshall-Smith Syndrome Symptoms, Diagnosis, Treatments

Marshall-Smith Syndrome: Introduction. Marshall-Smith Syndrome: A rare genetic disorder characterized by accelerated growth and maturation, shallow orbits and broad middle bones of fingers. More detailed information about the symptoms, causes, and treatments of Marshall-Smith …

What is MSS? – marshallsmith.org

The Marshall-Smith syndrome (MSS) is a very infrequently described syndrome. The syndrome has been described for the first time in 1971. Since then, about 50 children and adults with the syndrome are known in the medical literature worldwide. The syndrome is characterized by: – …

Marshall-Smith Syndrome – Social Security Administration

DI 23022.231 Marshall-Smith Syndrome. DESCRIPTION Marshall-Smith Syndrome (MSS) is a genetic disorder characterized by accelerated skeletal maturation, failure to thrive, respiratory difficulties, dysmorphic facial features, and moderate to severe developmental delay with absent or limited speech and unusual behavior.

Marshall-Smith syndrome | Radiology Reference Article

Marshall-Smith syndrome (MSS) is a rare genetic syndrome primarily comprising of the triad of facial dysmorphism, failure to thrive and accelerated osseous maturation 5. Many cases however have wider clinical spectrum. Article:

Marshall-Smith Syndrome – symptoma.com

Marshall-Smith syndrome is a rare congenital condition, characterized by advanced bone age, facial anomalies and relative failure to thrive. We report a newborn male with Marshall-Smith syndrome and summarize 21 previously reported cases.

Home – marshallsmith.org

The Marshall-Smith syndrome (MSS) is a very infrequently described syndrome. The syndrome has been described for the first time in 1971. Since then, about 50 children and adults with the syndrome are known in the medical literature worldwide. Read more

Definition of Marshall-Smith syndrome – MedicineNet

Marshall-Smith syndrome: A disorder characterized by advanced bone age at birth, broad forehead, prominent eyes, and small chin. There is difficulty feeding, failure to thrive , retarded psychomotor development, and predisposition to respiratory infection.

Marshall-Smith Syndrome: Reaching for the STARS

The child had Marshall-Smith syndrome (MSS), a very rare childhood condition which involves specific facial characteristics, respiratory problems, bone maturation that is advanced for the child’s age (for example, in 1993 a newborn with MSS was found to have the ‘bone age’ of a three year-old child).

(PDF) Marshall-Smith Syndrome: a distinct entity

Marshall-Smith syndrome (MSS) is a distinctive entity of unknown etiology with fewer than 50 patients described in the medical literature to date.

Marshall-Smith syndrome – The Full Wiki

Marshall-Smith Syndrome, discovered in 1971 (Marshall, Graham, Scott, Boner, & Smith), is characterized by unusual accelerated skeletal maturation (usually starting before birth) and symptoms like conspicuous physical characteristics, respiratory difficulties, and mental retardation. Cases described in the literature show a clinical variabililty regarding related symptoms.

ICD-10: GroupMajor.minor

Marshall-Smith syndrome | Connective Tissue Gene Tests

Marshall-Smith syndrome Marshall-Smith syndrome is characterized by accelerated linear growth and skeletal maturation, typical facial features, psychomotor delay, and respiratory insufficiency. Clinical findings in Sotos syndrome 2 are similar to Marshall-Smith syndrome. read more

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