Multiple lentigines syndrome. Case report and review of the literature

The American Journal of Medicine

Volumn 60, Issue 3, 1976, Pages 447-456

  Voron, David A ^a   Hatfield, Hayes H ^a   Kalkhoff, Ronald K ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT INHERITANCE; CHILD; DIAGNOSIS; ETIOLOGY; HISTOLOGY; MAJOR CLINICAL STUDY;

ADOLESCENT; ENDOCRINE GLANDS; GENES, DOMINANT; GENITALIA, MALE; HEART DEFECTS, CONGENITAL; HUMAN; MALE; NERVOUS SYSTEM DISEASES; PULMONARY VALVE STENOSIS; SYNDROME;

EID: 0017251174     PISSN: 00029343     EISSN: None     Source Type: Journal    
DOI: 10.1016/0002-9343(76)90764-6     Document Type: Review

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12. Lentiginosis profusa syndrome (multiple lentigines syndrome)
13. Lentiginosis profusa syndrome
14. Multiple symmetrical moles with psychic and somatic infantilism and genital hypoplasia first male case of a new syndrome
15. Progressive profusa lentiginosis, progressive cardiomyopathy, short stature with delayed puberty, mental retardation, or psychic infantilism, and other developmental abnormalities: a new familial syndrome
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17. Progressive cardiomyopathic lentiginosis: first report of autopsy findings in a recently recognized inheritable disorder (autosomal dominant)
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21. The multiple lentigines syndrome
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26. Congenital deafness with multiple lentigines in mother and daughter
27. Stenose de l'artere pulmonaire taches cutanes pigmentaires et anomalies du squelette. Quatre observations
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29. Rare case of the multiple micromaculous rash syndrome
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38. skeletal anomalies in genetically determined congenital heart disease
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