As ALDH18A1, which encodes for delta1‐pyrroline‐5‐carboxylate synthase (P5CS), is found to be responsible for this condition and a missense mutation (more commonly), it has been linked to symptoms like worsening nerve damage, cataracts, loose skin, joint problems, and metabolic issues; all of which can be found in ADCL type 3 [3]. The gene discussed is ALDH18A1; the disease is cataract.