Alport's syndrome and achalasia
โ Scribed by Heinz E. Leichter; Jorge Vargas; Arthur H. Cohen; Marvin Ament; Isidro B. Salusky
- Publisher
- Springer
- Year
- 1988
- Tongue
- English
- Weight
- 596 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0931-041X
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Sjรถgren's syndrome (SS) in its classical form, which includes keratoconjunctivitis sicca, xerostomia and recurrent enlargement of the salivary glands, is associated with a connective tissue disease in at least half the patients. According to the present study of three patients with SS, achalasia and
Four kindreds segregating for Alport's syndrome (ASLN) compatible with a X-linked inheritance were studied for linkage with polymorphic markers of the human X chromosome. No recombinant was observed between the ASLN locus and the DXS101 and DXS94 loci, the maximum lod scores were z = 3.93 and 3.50 r