The Human Phenotype Ontology (HPO) provides the following list of features that have been reported in people with this condition. Much of the information in the HPO comes from Orphanet, a European rare disease database. If available, the list includes a rough estimate of how common a feature is (its frequency). Frequencies are based on a specific study and may not be representative of all studies. You can use the MedlinePlus Medical Dictionary for definitions of the terms below.
|Signs and Symptoms||Approximate number of patients (when available)|
|Accelerated skeletal maturation||90%|
|Bowing of the long bones||90%|
|Depressed nasal bridge||90%|
|Slender long bone||90%|
|Abnormality of the tongue||50%|
|Conductive hearing impairment||50%|
|Reduced bone mineral density||50%|
|Aplasia/Hypoplasia of the cerebellum||7.5%|
|Agenesis of corpus callosum||-|
|Atria septal defect||-|
|Autosomal dominant inheritance||-|
|Bullet-shaped middle phalanges of the hand||-|
|Death in childhood||-|
|Decreased body weight||-|
|Distal widening of metacarpals||-|
|Failure to thrive||-|
|Hypoplasia of the odontoid process||-|
|Large sternal ossification centers||-|
|Obstructive sleep apnea||-|
|Patent ductus arteriosus||-|
|Prominence of the premaxilla||-|
|Recurrent aspiration pneumonia||-|
|Short distal phalanx of finger||-|
|Short mandibular rami||-|
Nonprofit support and advocacy groups bring together patients, families, medical professionals, and researchers. These groups often raise awareness, provide support, and develop patient-centered information. Many are the driving force behind research for better treatments and possible cures. They can direct people to research, resources, and services. Many groups also have experts who serve as medical advisors. Visit their website or contact them to learn about the services they offer. Inclusion on this list is not an endorsement by GARD. Suggest an organization to add.
Living with a genetic or rare disease can impact the daily lives of patients and families. These resources can help families navigate various aspects of living with a rare disease.
These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.
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I am a speech language pathologist with a child affected by Marshall-Smith syndrome on my caseload. Do the symptoms of this syndrome vary widely between patients? Is there any information regarding speech / language prognosis for these children? See answer