Gastrointestinal problems in a child with dyskeratosis congenita

American Journal of Gastroenterology

Volumn 91, Issue 6, 1996, Pages 1271-1272

  Berezin, Stuart ^a   Schwarz, Steven M ^a   Slim, Michel S ^a   Beneck, Debra ^a   Brudnicki, Adele R ^a   Medow, Marvin S ^a  

^a NEW YORK MEDICAL COLLEGE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ABDOMINAL PAIN; ARTICLE; CASE REPORT; DYSKERATOSIS CONGENITA; DYSPHAGIA; DYSTROPHY; GASTROINTESTINAL BIOPSY; GENETIC PREDISPOSITION; HUMAN; HYPERHIDROSIS; HYPERPIGMENTATION; LEUKOPLAKIA; MALE; PANCYTOPENIA; PRESCHOOL CHILD; PRIORITY JOURNAL; SYMPTOMATOLOGY; VOMITING;

CHILD; GASTROINTESTINAL DISEASES; HUMANS; HYPERPIGMENTATION; LEUKOPLAKIA; LINKAGE (GENETICS); MALE; NAIL DISEASES; PANCYTOPENIA; SYNDROME; X CHROMOSOME;

EID: 0029884355     PISSN: 00029270     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Womer R, Clark JE, Wood P, et al. Dyskeratosis congenita: Two examples of this multi-system disorder. Pediatrics 1983;71:603-9.
2. Sondheimer JM. Continuous monitoring of distal esophageal pH: A diagnostic test for gastroesophageal reflux in infants. J Pediatr 1980; 96:804-7.
3. Euler AR, Byrne WJ. Twenty-four hour esophageal intraluminal pH probe testing: A comparative analysis. Gastroenterology 1981;80:957-61.
4. Sirinarin C, Trowbridge A. Dyskeratosis congenita: Clinical features and genetic aspects. J Med Genet 1975;12:339-53.
5. Steier W, Van Voolen A, Selmanowitz V. Dyskeratosis congenita: Relationship to Fanconi's anemia. Blood 1972;39:510-20.
6. Brown KC, Kelly TE, Myers BM. Gastrointestinal involvement in a woman with dyskeratosis congenita. Dig Dis Sci 1993;38:181-4.