Leopard syndrome

LEOPARD syndrome: A genetic syndrome transmitted in an autosomal dominant manner that is named for its characteristic features: ...

LEOPARD syndrome is an autosomal dominant syndrome consisting of multiple lentigines and junctional nevi, electrocardiographic changes, ocular hypertelorism, pulmonary and subaortic stenosis, abnormalities of the genitalia, ...

Alternate Names : Leopard syndrome
Definition
Multiple lentigines syndrome is an inherited disorder identified by an increased number of lentigines (freckle-like spots).

Leopard syndrome
Causes, incidence, and risk factors
Multiple lentigines syndrome is inherited as an autosomal dominant trait. People with this condition have large numbers of lentigines.

Leopard syndrome
Leprosy
Leptospirosis
Lesch-Nyhan syndrome
Letterer-Siwe disease
Leukemia
Leukemia - acute childhood (ALL)
Leukemia - acute granulocytic
Leukemia - acute myeloid (AML)
Leukemia - chronic granulocytic (CML) ...

Dichloride, Alcuronium, Factor, Angiogenic, Galactorrheas, Gastric Contents Aspiration, Genes, MTS1, Genome Project, Human, Giant Cell, Multinucleated, Glioblastoma, Giant Cell, Grand Mal Convulsions, Health Systems Plans, Larvae, LEOPARD Syndrome, ...

Leopard syndrome (multiple lentigines)
Mohr syndrome
Morquio syndrome
Multiple lentigines syndrome
Multiple synostosis syndrome
Osteogenesis imperfecta
Otosclerosis
Robinson type ectodermal dysplasia
Stickler syndrome ...

leopard syndrome
leriche's syndrome
Leri-Weill syndrome
Lermoyez' syndrome
Lesch-Nyhan syndrome
leukocyte-adhesion deficiency syndrome
Lev's syndrome
Libman-Sacks syndrome
Li-Fraumeni cancer syndrome
Li-Fraumeni syndrome ...

Leopard syndrome
McCune Albright syndrome
Multiple endocrine neoplasia syndrome type 2B
Multiple intradermal nevi
Multiple lipomatosis
NF1 and NF2 share certain symptoms, and must be differentiated from each other
Proteus syndrome ...

Nonsolar lentigines are sometimes associated with systemic disorders, such as Peutz-Jeghers syndrome (in which profuse lentigines of the lips occur), multiple lentigines syndrome (Leopard syndrome), or xeroderma pigmentosum.

protein tyrosine phosphatase: PTEN (Bannayan-Riley-Ruvalcaba syndrome, Lhermitte-Duclos disease, Cowden syndrome, Proteus-like syndrome) Â- MTM1 (X-linked myotubular myopathy) Â- PTPN11 (Noonan syndrome 1, LEOPARD syndrome, Metachondromatosis) ...

There seems to be an association with multiple lentigines, and there have been cases reported in patients with a definite diagnosis of Noonan syndrome, neurofibromatosis type I, and Leopard syndrome.

LEOPARD Syndrome (9 images)
Lepra Lepromatosa (1 images)
Lepra Tuberculosa (0 images)
Leprechaunism Syndrome (5 images)
Lesch-Nyhan Syndrome / Pseudo- Lesch-Nyhan Syndrome (0 images)
Leser-Trélat Syndrome (0 images) ...

See also: Cancer, Sclerosis, Deficiency, Myalgia, Bacterial