Expanding the phenotype of oculoectodermal syndrome: Possible relationship to encephalocraniocutaneous lipomatosis

American Journal of Medical Genetics, Part A

Volumn 143, Issue 24, 2007, Pages 2959-2962

  Ardinger, Holly H ^a,b   Horii, Kimberly A ^a,b   Begleiter, Michael L ^a,b  

^a CHILDREN S MERCY HOSPITAL   (United States)

^b UNIVERSITY OF MISSOURI KANSAS CITY SCHOOL OF MEDICINE   (United States)

Author keywords

Alopecia; Aplasia cutis congenital; Epibulbar dermoid; Smooth muscle hamartoma

Indexed keywords

ALOPECIA; BRAIN TUMOR; CASE REPORT; CLINICAL FEATURE; CONFERENCE PAPER; FEMALE; HUMAN; HUMAN TISSUE; INFANT; LIPOMATOSIS; MALE; MUSCLE HEMATOMA; NUCLEAR MAGNETIC RESONANCE IMAGING; OCULOECTODERMAL SYNDROME; PHENOTYPE; PRIORITY JOURNAL; SKIN APLASIA; SKIN DISEASE; TERATOMA;

ABNORMALITIES, MULTIPLE; ALOPECIA; BRAIN; CHILD; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; EYE ABNORMALITIES; FACIES; FEMALE; HAMARTOMA; HUMANS; INFANT; INFANT, NEWBORN; LIPOMATOSIS; MALE; NEUROCUTANEOUS SYNDROMES; PHENOTYPE; SKIN ABNORMALITIES; SYNDROME;

EID: 37249058869     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31969     Document Type: Conference Paper

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