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Illness finder is a diagnostic medicine tool for educational purpose that looks up your patients' health conditions or symptoms and diagnosis and find diseases or illnesses based on chosen gender, age, risk factors, illness, signs, symptoms and prevalence. Illnessfinder is inspired by Evidence based medicine (EMB) and healthcare that aims to apply the best (most reliable) knowledge that is available at decision time. Illnessfinder aims to free up time for the therapeutic dialogue and ensure quality at the evidence based practice, uniting proven medical findings and clinical evidence with systematised data technology.
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| LEOPARD Syndrome | Legal notice |
Other terms
LEOPARD Syndromes,Syndrome, LEOPARD,Syndromes, LEOPARD,Multiple Lentigines Syndrome,Lentigines Syndrome, Multiple,Lentigines Syndromes, Multiple,Multiple Lentigines Syndromes,Syndrome, Multiple Lentigines,Syndromes, Multiple Lentigines
Description
LEOPARD Syndrome: An autosomal dominant disorder with an acronym of its seven features (LENTIGO; ELECTROCARDIOGRAM abnormalities; ocular HYPERTELORISM; PULMONARY STENOSIS; abnormal genitalia; retardation of growth; and DEAFNESS or SENSORINEURAL HEARING LOSS). This syndrome is caused by mutations of PTPN11 gene encoding the non-receptor PROTEIN TYROSINE PHOSPHATASE, type 11, and is an allelic to NOONAN SYNDROME. Features of LEOPARD syndrome overlap with those of NEUROFIBROMATOSIS 1 which is caused by mutations in the NEUROFIBROMATOSIS 1 GENES.
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- Craniofacial Abnormalities
- Heart Defects, Congenital
- Pulmonary Valve Stenosis
- Abnormalities, Multiple
- Heart Defects, Congenital
- Craniofacial Abnormalities
- Lentigo
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