Infantile McCune-Albright syndrome

Pediatric Dermatology

Volumn 18, Issue 6, 2001, Pages 504-506

  Davies, Justin H ^a,c   Barton, John S ^a   Gregory, John W ^b   Mills, Caroline ^a  

^a ROYAL GWENT HOSPITAL   (United Kingdom)

^b CARDIFF UNIVERSITY   (United Kingdom)

^c NONE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GUANINE NUCLEOTIDE BINDING PROTEIN;

ALBRIGHT SYNDROME; ARTICLE; BONE DYSPLASIA; CARDIOPULMONARY INSUFFICIENCY; CASE REPORT; DISEASE ASSOCIATION; ENDOCRINE DISEASE; FACE; FAILURE TO THRIVE; FIBROUS DYSPLASIA; GENE MUTATION; HUMAN; HYPERCORTISOLISM; HYPERTHYROIDISM; INFANT; LIMB; MALE; PRIORITY JOURNAL; SKIN PIGMENTATION; TRUNK;

CAFE-AU-LAIT SPOTS; CUSHING SYNDROME; FIBROUS DYSPLASIA, POLYOSTOTIC; HUMANS; HYPERTHYROIDISM; INFANT; MALE;

EID: 0035702890     PISSN: 07368046     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1525-1470.2001.1862003.x     Document Type: Article

References (9)

1. Melanocytic macules following Blashcko's lines in McCune-Albright syndrome
2. A case of neonatal McCune-Albright syndrome with Cushing syndrome and hyperthyroidism
3. Cushing's syndrome caused by nodular adrenal hyperplasia in children with McCune-Albright syndrome
4. S
5. Activating mutations of the stimulatory G protein in the McCuneAlbright syndrome
6. Activating mutation in the stimulatory guanine nucleotide-binding protein in an infant with Cushing's syndrome and nodular adrenal hyperplasia
7. Sα in McCune-Albright syndrome causes skin pigmentation by tyrosinase gene activation on affected melanocytes
8. Lethal genes surviving by mosaicism: A possible explanation for sporadic birth defects involving the skin
9. Mitogenic and melanogenic stimulation of normal human melanocytes by melanotropic peptides