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Limb-mammary syndrome

Also Known As:
Mammary hypoplasia, ectrodactyly, and other hand/foot anomalies
Networked: 13 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Experts

1. van Bokhoven, Hans: 2 articles (05/2007 - 04/2002)
2. Brunner, Han G: 2 articles (10/2002 - 04/2002)
3. Hamel, B C: 2 articles (09/2001 - 02/2001)
4. Duijf, P H: 2 articles (09/2001 - 02/2001)
5. van Bokhoven, H: 2 articles (09/2001 - 02/2001)
6. Vanmolkot, K R: 2 articles (09/2001 - 02/2001)
7. Brunner, H G: 2 articles (09/2001 - 02/2001)
8. Du, Yangge: 1 article (01/2015)
9. Yin, Wei: 1 article (01/2015)
10. Song, Yaling: 1 article (01/2015)

Related Diseases

1. Ectodermal Dysplasia (Aplasia Cutis Congenita)
01/01/2007 - "Moreover, we show that transcription of Dlx3 is abrogated by mutations in the sterile alpha-motif (SAM) domain of p63 that are associated with ankyloblepharon-ectodermal dysplasia-clefting (AEC) dysplasias, but not by mutations found in ectrodactylyectodermal dysplasia-cleft lip/palate (EEC), Limb-mammary syndrome (LMS) and split hand-foot malformation (SHFM) dysplasias. "
08/01/2014 - "It can affect either sex and is mostly part of syndromes including other congenital or ectodermal anomalies, such as limb-mammary syndrome, scalp-ear-nipple syndrome, or ectodermal dysplasias. "
11/01/2011 - "Its clinical phenotype is similar to ectrodactyly-ectodermal dysplasia-cleft lip/palate (EEC) and limb-mammary syndrome (LMS), and differs from these disorders mainly by the absence of cleft lip and/or palate. "
08/01/2010 - "To test whether TP63 is the disease-causative gene for these phenotypes in Chinese, we recruited two Chinese Ectrodactyly-Ectodermal-dysplasia-Cleft lip/palate syndrome (EEC) cases and a Limb-Mammary-Syndrome (LMS) patient to carry out TP63 gene sequencing. "
01/01/2004 - "The condition appears to be genetically heterogeneous and recently it has been demonstrated that mutations in the p63 gene, a homologue of the tumor suppressor gene p53, are the cause of at least four autosomal dominant genetic syndromes which feature ectrodactyly: ectrodactyly, ectodermal dysplasia, and facial clefting (EEC), split hand/split foot malformation (SHFM), limb-mammary syndrome (LMS), and acro-dermato-ungual-lacrimal-tooth syndrome (ADULT). "
2. Cleft Lip (Harelip)
3. Cleft Palate (Palate, Cleft)
4. Hypohidrosis
5. Anodontia

Related Drugs and Biologics

1. Ectrodactyly
2. Ectrodactyly-cleft lip/palate syndrome
3. Propping Zerres syndrome
4. Zlotogora syndrome
5. Scalp ear nipple syndrome
6. Hay-Wells syndrome
7. Rapp-Hodgkin syndrome