Griscelli syndrome: A new phenotype with circumscribed pigment loss?

Dermatology Online Journal

Volumn 13, Issue 2, 2007, Pages

  Kharkar, Vidya ^a   Pande, Sushil ^a   Mahajan, Sunanda ^a   Dwiwedi, Ravishankar ^a   Khopkar, Uday ^a  

^a KEM HOSPITAL   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ASCORBIC ACID;

ADULT; ANAMNESIS; ARTICLE; BONE MARROW EXAMINATION; CASE REPORT; CHEDIAK HIGASHI SYNDROME; CLINICAL FEATURE; EXERCISE TEST; EYEBROW; EYELASH; FEMALE; GRISCELLI SYNDROME; HAIR DISCOLORATION; HUMAN; HUMAN CELL; KARYOTYPE 46,XX; KARYOTYPING; LABORATORY TEST; NUCLEAR MAGNETIC RESONANCE IMAGING; OPHTHALMOSCOPY; PATIENT CARE; PATIENT COUNSELING; PHENOTYPE; PHYSICAL EXAMINATION; SCALP HAIR; SKIN PIGMENTATION; AGAMMAGLOBULINEMIA; ALBINISM; CHROMOSOME 15; GENETICS; HEPATOMEGALY; HOSPITALIZATION; IMMUNE DEFICIENCY; MENTAL DEFICIENCY; PANCYTOPENIA; PROGNOSIS; RISK ASSESSMENT; SPLENOMEGALY; SYNDROME;

ADULT; AGAMMAGLOBULINEMIA; ALBINISM; CHROMOSOMES, HUMAN, PAIR 15; FEMALE; HEPATOMEGALY; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; MENTAL RETARDATION; PANCYTOPENIA; PHENOTYPE; PROGNOSIS; RISK ASSESSMENT; SEVERITY OF ILLNESS INDEX; SPLENOMEGALY; SYNDROME;

EID: 34248136974     PISSN: None     EISSN: 10872108     Source Type: Journal    
DOI: None     Document Type: Article

References (11)

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