Multiple lentigines syndrome

Multiple lentigines syndrome
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Multiple lentigines syndrome is inherited as an autosomal dominant trait. People with this condition have large numbers of lentigines. Lentigines are skin markings that are somewhat darker than true freckles. They are present from birth.

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

Some of the many genetic disorders that can cause deafness include osteogenesis imperfecta, Trisomy 13 S and multiple lentigines syndrome.

LEOPARD syndrome is the most common name for the disorder. It is also known as multiple lentigines syndrome, Gorlin syndrome II, cardio-cutaneous syndrome, lentiginosis profusa syndrome, progressive cardiomyopathic lentiginosis.

Multiple lentigines syndrome
Multiple synostosis syndrome
Osteogenesis imperfecta
Otosclerosis
Robinson type ectodermal dysplasia
Stickler syndrome
Taybi oto-palato-digital syndrome
Treacher Collins syndrome
Trisomy 13
Waardenburg syndrome ...

A family history of certain hereditary or congenital syndromes such as Noonan's, Waardenburg syndrome, Multiple lentigines syndrome, or Kartagener 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.

multiple lentigines syndrome
multiple mucosal neuroma syndrome
munchausen syndrome
munchhausen syndrome
murine acquired immunodeficiency syndrome
myasthenic syndrome
myelodysplastic syndrome
myofacial pain-dysfunction syndrome ...

See also: Leopard syndrome, Stenosis, Cancer, Deficiency, Deafness