Search on: ROTHMUND-THOMSON SYNDROME 
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Descriptor English:   Rothmund-Thomson Syndrome 
Descriptor Spanish:   Síndrome Rothmund-Thomson 
Descriptor Portuguese:   Síndrome de Rothmund-Thomson 
Synonyms English:   Poikiloderma Congenitale  
Tree Number:   C16.131.831.775
C16.320.850.765
C16.614.760
C17.800.804.775
C17.800.827.775
C18.452.284.760
Definition English:   An autosomal recessive syndrome occurring principally in females, characterized by the presence of reticulated, atrophic, hyperpigmented, telangiectatic cutaneous plaques, often accompanied by juvenile cataracts, saddle nose, congenital bone defects, disturbances in the growth of HAIR; NAILS; and TEETH; and HYPOGONADISM. 
History Note English:   2006 (1964) 
Allowable Qualifiers English:  
blood cerebrospinal fluid
chemically induced classification
complications diet therapy
diagnosis drug therapy
economics ethnology
embryology enzymology
epidemiology etiology
genetics history
immunology metabolism
microbiology mortality
nursing pathology
prevention & control physiopathology
parasitology psychology
radiography rehabilitation
radionuclide imaging radiotherapy
surgery therapy
ultrastructure urine
ultrasonography veterinary
virology  
Record Number:   11468 
Unique Identifier:   D011038 

Occurrence in VHL:
 

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