WordNet

gradually advancing in extent
a tense of verbs used in describing action that is on-going (同)progressive tense, imperfect, imperfect tense, continuous tense
favoring or promoting reform (often by government action) (同)reformist, reform-minded
(of a card game or a dance) involving a series of sections for which the participants successively change place or relative position; "progressive euchre"; "progressive tournaments"
(of taxes) adjusted so that the rate increases as the amount of income increases
advancing in severity; "progressive paralysis"
favoring or promoting progress; "progressive schools"

PrepTutorEJDIC

(行列などが)『前進する』,進んで行く / (事態が)進展する,進行する / 『進歩的な』,革新的な / (病気・暴力などが)次第に悪くなる(広がる) / (課税が)累進的な / (文法で)進行[形]の / 進歩的な人,革新主義者
世襲の,親譲りの / 遺伝的な,遺伝性の

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Osteoarthritis at young age, a diagnostic challenge: a case of stickler syndrome.

de Wergifosse I1, Westhovens R1.
The open rheumatology journal.Open Rheumatol J.2014 Dec 19;8:100-2. doi: 10.2174/1874312901408010100. eCollection 2014.
A young woman presents with severe polyarticular osteoarthritis with relevant family history potentially suggesting a hereditary disease. Previously, the patient's mother had been diagnosed with rheumatoid arthritis and reported to have suffered from some locomotor problems. Careful clinical evaluat
PMID 25598853

The clinical effectiveness and safety of prophylactic retinal interventions to reduce the risk of retinal detachment and subsequent vision loss in adults and children with Stickler syndrome: a systematic review.

Carroll C1, Papaioannou D, Rees A, Kaltenthaler E.
Health technology assessment (Winchester, England).Health Technol Assess.2011 Apr;15(16):iii-xiv, 1-62. doi: 10.3310/hta15160.
BACKGROUND: Stickler syndrome, also known as hereditary progressive arthro-ophthalmopathy, is an inherited progressive disorder of the collagen connective tissues. Manifestations include short-sightedness, cataracts, retinal problems leading to retinal detachment and possible blindness. This is prin
PMID 21466760

Clinical variability of Stickler syndrome: role of exon 2 of the collagen COL2A1 gene.

Donoso LA1, Edwards AO, Frost AT, Ritter R 3rd, Ahmad N, Vrabec T, Rogers J, Meyer D, Parma S.
Survey of ophthalmology.Surv Ophthalmol.2003 Mar-Apr;48(2):191-203.
Stickler syndrome (progressive arthro-ophthalmopathy) is a genetically heterogeneous disorder resulting from mutations in at least three collagen genes. The most common disease-causing gene is COL2A1, a 54-exon-containing gene coding for type II collagen. At least 17 different mutations causing Stic
PMID 12686304