Hallermann's Syndrome (Hallermann Streiff Syndrome)
An oculomandibulofacial syndrome principally characterized by dyscephaly (usually brachycephaly), parrot nose, mandibular hypoplasia, proportionate nanism, hypotrichosis, bilateral congenital cataracts, and microphthalmia. (Dorland, 27th ed)
Also Known As:
Hallermann Streiff Syndrome; Syndrome, Hallermann-Streiff; Hallermann Syndrome; Hallermanns Syndrome; Syndrome, Hallermann's; Hallermann-Streiff Syndrome
Networked: 15
relevant articles (1 outcomes,
0 trials/studies)
Relationship Network
Disease Context: Research Results
Related Diseases
Experts
1. | Liu, Lei:
1 article
(08/2014)
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2. | Sun, Quan:
1 article
(08/2014)
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3. | Li, Kaide:
1 article
(08/2014)
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4. | Abrams, Charles K:
1 article
(08/2012)
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5. | Scherer, Steven S:
1 article
(08/2012)
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6. | Bhagat, Shubhada:
1 article
(05/2012)
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7. | Krishna, Handattu Mahabaleswara:
1 article
(05/2012)
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8. | Vinodhadevi, Vijayakumar:
1 article
(05/2012)
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9. | Parikh, Shilpa:
1 article
(01/2012)
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10. | Gupta, Swati:
1 article
(01/2012)
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Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Hallermann's Syndrome:
1. | disodium salt olean-11,13(18)-diene-3,30-diol dihemiphthalateIBA
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2. | Gracile bone dysplasiaIBA
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3. | Arthrogryposis multiplex congenitaIBA
01/01/1980
- " These included 2 with trisomy 13 (including a mosaic), 3 with trisomy 18 (including 1 mosaic), 16 with trisomy 21 (including 1 mosaic), 1 with cri-du-chat syndrome, 1 with 5p partial trisomy, 1 with Hallermann-Streiff syndrome, 1 with Treacher-Collins syndrome, 1 with achodroplasia, 2 with arthrogryposis multiplex congenita, 1 with hemihypertrophy, 1 with Wiedemann-Beckwith syndrome, 1 with asplenia syndrome, 1 with Klippel-Trenaunay-Weber syndrome, and 1 with probable Marfan's syndrome. "
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4. | Hereditary renal agenesisIBA
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5. | Patau syndromeIBA
01/01/1980
- " These included 2 with trisomy 13 (including a mosaic), 3 with trisomy 18 (including 1 mosaic), 16 with trisomy 21 (including 1 mosaic), 1 with cri-du-chat syndrome, 1 with 5p partial trisomy, 1 with Hallermann-Streiff syndrome, 1 with Treacher-Collins syndrome, 1 with achodroplasia, 2 with arthrogryposis multiplex congenita, 1 with hemihypertrophy, 1 with Wiedemann-Beckwith syndrome, 1 with asplenia syndrome, 1 with Klippel-Trenaunay-Weber syndrome, and 1 with probable Marfan's syndrome. "
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6. | Dermochondrocorneal dystrophy of FrançoisIBA
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Therapies and Procedures