Universal dyschromatosis, small stature and high‐tone deafness

Clinical and Experimental Dermatology

Volumn 2, Issue 1, 1977, Pages 45-48

  RYCROFT, R J G ^a   CALNAN, C D ^a   WELLS, R S ^b  

^a ST THOMAS HOSPITAL   (United Kingdom)

^b GUY S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BODY HEIGHT; CHILD; CONSANGUINEOUS MARRIAGE; DIAGNOSIS; DYSCHROMATOSIS; HEARING IMPAIRMENT; HYPERPIGMENTATION; HYPOPIGMENTATION; MAJOR CLINICAL STUDY;

CASE REPORT; CHILD; DEAFNESS; FEMALE; GROWTH DISORDERS; HUMAN; PIGMENTATION DISORDERS;

EID: 0017737929     PISSN: 03076938     EISSN: 13652230     Source Type: Journal    
DOI: 10.1111/j.1365-2230.1977.tb01536.x     Document Type: Article

References (15)

1. A familial pigmentary anomaly
2. Dyskeratosis congenita and familial pancytopenia
3. Erythema dyschromicum perstans, a hitherto undescribed skin disease
4. Universal dyschromatosis
5. Dermatopathia pigmentosa reticularis
6. A propose de ‘l’ Incontinenta pigmentt, delimitation de deux syndromes differents figurant sous la même terme
7. Über eine noch nicht beschriebene Pigmentanomalie, Dyschromatosis universalis hereditaria
8. Symmetrische Pigmentanomalie der Extremitäten
9. Familial pigmentation with dystrophy of the nails
10. Diffuse pigmentation in brothers
11. Dyschromatosis universalis hereditaria in 5 generations
12. A hitherto undescribed generalized pigmentation of the skin appearing in infancy in brother and sister
13. Generalized naevoid pigmentation
14. Dyschromatosis symmetrica hereditaria