The H syndrome: A genodermatosis characterized by indurated, hyperpigmented, and hypertrichotic skin with systemic manifestations

Journal of the American Academy of Dermatology

Volumn 59, Issue 1, 2008, Pages 79-85

  Molho Pessach, Vered ^a   Agha, Ziad ^a   Aamar, Suhail ^a   Glaser, Benjamin ^a   Doviner, Victoria ^a   Hiller, Nurith ^a   Zangen, David Haim ^a   Raas Rothschild, Annick ^a   Ben Neriah, Ziva ^a   Shweiki, Shaher ^b   Elpeleg, Orly ^a   Zlotogorski, Abraham ^a  

^a HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

^b Makassed Islamic Hospital   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AZOOSPERMIA; CELL INFILTRATION; CHILD; CLINICAL ARTICLE; CLINICAL EXAMINATION; COMPARATIVE STUDY; CONSANGUINITY; CONTROLLED STUDY; FEMALE; GENODERMATOSIS; GROWTH HORMONE DEFICIENCY; HEART DISEASE; HEPATOSPLENOMEGALY; HISTIOCYTE; HISTOLOGY; HUMAN; HYPERGONADOTROPIC HYPOGONADISM; HYPERPIGMENTATION; HYPERTRICHOSIS; LABORATORY TEST; MALE; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SCROTUM; SEBORRHEIC KERATOSIS; SHORT STATURE;

ADOLESCENT; ADULT; BIOPSY; CONSANGUINITY; FEMALE; FIBROSIS; GENITAL DISEASES, MALE; HEARING LOSS, SENSORINEURAL; HEART DEFECTS, CONGENITAL; HEPATOMEGALY; HUMANS; HYPERPIGMENTATION; HYPERTRICHOSIS; LYMPH NODES; MALE; PHENOTYPE; SKIN; SKIN DISEASES, GENETIC; SPLENOMEGALY; SYNDROME;

EID: 45049088360     PISSN: 01909622     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jaad.2008.03.021     Document Type: Article

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