1                                              HHCS cataract is due to numerous small opacities, predom

2                                              HHCS is a noteworthy example of a human genetic disorder

3                                              HHCS is an autosomal dominant condition caused by mutati

4                                              HHCS was diagnosed in five members of one family who had

5                                              HHCS was diagnosed in this study in one of the first fam

6 l and electron microscopic analyses of human HHCS lens aspirate.

7 d States, and the basis of lens opacities in HHCS was determined.

8         The excessive ferritin production in HHCS patients arises from aberrant regulation of L-ferri

9 onstrates the need for clinical awareness of HHCS as a cause of hyperferritinemia in the absence of i

10 se IREs has also revealed that although some HHCS mutations lead to changes in the stability and seco

11 editary hyperferritinemia cataract syndrome (HHCS) is a genetic disease defined by cataracts, hyperfe

12 editary hyperferritinemia-cataract syndrome (HHCS) is a novel genetic disorder characterized by eleva

13 editary hyperferritinemia cataract syndrome (HHCS; OMIM #600886).

14 ious observations suggested that each unique HHCS mutation conferred a characteristic degree of hyper

15                     We report a patient with HHCS who was misdiagnosed and treated as having hemochro

16                                Patients with HHCS may be recognized by a family history of cataracts