2. Bloom Syndrome
Bloom-Torre-Mackacek Syndrome; BS; Dwarfism, Levi's Type; Short Stature and Facial Telangiectasis; Short Stature, Telangiectatic Erythema of the Face;
Healthline.com (OMS Preferred Provider)

3. Bloom syndrome - Educational resources - Information pages - Genetics Home Reference
These resources supplement the information in the Genetics Home Reference condition summary on Bloom syndrome.
MedlinePlus (Offsite)

4. Bloom syndrome - Genetics Home Reference
Bloom syndrome is an inherited disorder characterized by a high frequency of breaks and rearrangements in an affected person's chromosomes. People with Bloom syndrome are much smaller than average, and often have a high-pitched...
MedlinePlus (Offsite)

5. Bloom Syndrome / Family Village
Bloom's Syndrome is a very rare inherited genetic disorder, caused by a gene that does not function properly. This creates an unusually high number of breaks or instability along their chromosomes (the structures in the cells of our body that cont...
www.waisman.wisc.edu

6. Bloom Syndrome - AOL Health
It is possible that the main title of the report Bloom Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
www.aolhealth.com

7. Ocular Syndromes and Systemic Diseases: Bloom Syndrome
General : Autosomal recessive inheritance; male preponderance; usually low birth weight following full-term gestation; full-term, abnormally small children.
www.medrounds.org

8. Bloom Syndrome (Congenital Telangiectatic Erythema): eMedicine Dermatology
Bloom syndrome (congenital telangiectatic erythema) is a rare autosomal recessive disorder characterized by telangiectases and photosensitivity, growth deficiency of prenatal onset, variable degrees of immunodeficiency, and increased susceptibilit...
emedicine.medscape.com

9. Weill Cornell Medical Center | Bloom's Syndrome Registry
German, J.: Bloom’s syndrome. I. Genetical and clinical observations in the first twenty-seven patients. Amer. J. Hum. Genet. 21:196-227, 1969. Chaganti, R. S. K., Schonberg, S., and German, J.: A manyfold increase in sister chromatid exchanges in...
med.cornell.edu

10. Weill Cornell Medical Center | Bloom's Syndrome Registry
BSyn is genetically determined, inherited as a rare autosomal recessive trait – both sexes affected; sibs the only affecteds in a given family; parental consanguinity common. The gene mutated, which is named BLM, is located in band q26.1 on...
www.med.cornell.edu