91 top medical experts on syndromic 1 Microphthalmia across 9 countries and 5 U.S. states, including 13 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. syndromic 1 Microphthalmia: A rare X-linked inherited form of syndromic microphthalmia characterized by unilateral or bilateral microphthalmia (and/or clinical anophthalmia) with or without coloboma in addition to a range of extraocular manifestations such as microcephaly, malformed ears, dental abnormalities (i.e. irregular shape of incisors), skeletal anomalies (duplicated thumbs, syndactyly, clinodactyly, camptodactyly), urogenital anomalies (hypospadias, cryptorchidism, renal dysgenesis, hydroureter) and mild to severe intellectual disability. It is allelic to two disorders: oculofaciocardiodental syndrome and premature aging appearance-developmental delay-cardiac arrhythmia syndrome.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Lenz Dysmorphogenic Syndrome,  Lenz Syndrome,  Lenz dysplasia,  Lenz microphthalmia syndrome,  MCOPS1,  MCOPS4,  Microphthalmia Or Anophthalmos with Associated Anomalies,  Microphthalmia With Ankyloblepharon And Mental Retardation,  Microphthalmia or anophthalmos with associated anomalies (formerly),  Syndromic 4 Microphthalmia


  

        

                    


    Computing Expert Listing ...