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Multiple lentigines syndrome; LEOPARD syndrome; NSML DefinitionNoonan syndrome with multiple lentigines (NSML) is a rare inherited disorder. People with this condition have problems with the skin, head and face, inner ear, and heart. The genitals may also be affected. Noonan syndrome with multiple lentigines was formerly known as LEOPARD syndrome. CausesNSML is inherited as an autosomal dominant trait. This means the person only needs an abnormal gene from one parent in order to inherit the disorder. SymptomsThe former name of NSML of LEOPARD stands for the different problems (signs and symptoms) of this disorder:
NSML is similar to Noonan syndrome. However, the main symptom that tells apart the two conditions is that people with NSML have lentigines. Exams and TestsYour health care provider will perform a physical exam and listen to the heart with a stethoscope. Tests that may be done include:
TreatmentSymptoms are treated as appropriate. A hearing aid may be needed. Hormone treatment may be necessary at the expected time of puberty to cause the normal changes to occur. Laser, cryosurgery (freezing), or bleaching creams may help lighten some of the brown spots on the skin. Support GroupsMore information and support for people with LEOPARD syndrome and their families can be found at:
Possible ComplicationsComplications vary and include:
When to Contact a Medical ProfessionalContact your provider if there are symptoms of this disorder. Contact your provider for an appointment if you have a family history of this disorder and plan to have children. PreventionGenetic counseling is recommended for people with a family history of NSLM who want to have children. ReferencesJames WD, Elston DM, Treat JR, Rosenbach MA, Neuhaus IM. Melanocytic nevi and neoplasms. In: James WD, Elston DM, Treat JR, Rosenbach MA, Neuhaus IM, eds. Andrews' Diseases of the Skin: Clinical Dermatology. 13th ed. Philadelphia, PA: Elsevier; 2020:chap 30. Paller AS, Mancini AJ. Disorders of pigmentation. In: Paller AS, Mancini AJ, eds. Paller and Mancini – Hurwitz Clinical Pediatric Dermatology. 6th ed. Philadelphia, PA: Elsevier; 2022:chap 11. | |
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Review Date: 5/31/2023 Reviewed By: Ramin Fathi, MD, FAAD, Director, Phoenix Surgical Dermatology Group, Phoenix, AZ. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team. The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed medical professional should be consulted for diagnosis and treatment of any and all medical conditions. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. No warranty of any kind, either expressed or implied, is made as to the accuracy, reliability, timeliness, or correctness of any translations made by a third-party service of the information provided herein into any other language. © 1997- A.D.A.M., a business unit of Ebix, Inc. Any duplication or distribution of the information contained herein is strictly prohibited. | |