Date of commencement: February Principal Investigator Dr. Jayesh J. Sheth CASE RECORD FORM

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ICMR-FRIGE-MULTICENTRIC LSDs Project Foundation for Research in Genetics & Endocrinology [FRIGE], FRIGE House, Jodhpur Gam road, Satellite, Ahmedabad-380015 Tel no: 079-26921414, Fax no: 079-26921415 E-mail: jshethad1@gmail.com Date of commencement: February 2015-2018 Principal Investigator Dr. Jayesh J. Sheth CASE RECORD FORM Multicentric Collaborative Study of the Clinical, Bio-chemical & Molecular characterization of lysosomal storage disorders (LSDs) in India- The initiative for research in LSDs Date: CRF No: FRIGE Reference No: Patient s Name: Address: Tel: No: Native Place address: Referred By: Self/relatives/other patients/family doctor/pediatrician/gynecologist/neurologist/ any other specialist (please specify) Age: Yrs. Body Weight (In Kg): Height (cms): Sex: M/F Upper Segment/ Lower Segment Ratio (cms): Head Circumference (cms): Mid Arm Circumference (cms): Age of Onset of Symptoms: Chest Circumference (cms): At Birth Birth to six months Six months to one year one year to 3 years later 1

Presenting Symptoms: Delayed milestones Convulsions Coarse features Growth retardation Skeletal abnormality Family history of LSD Any Other [Please specify] Diagnosis and Complications (If Any): Sickness/ Symptoms Date of diagnosis Current status (Controlled/ Uncontrolled) Current Medications (Drug/Dose/Duration Family History: Name of the Mother: Age: Yrs Name of the Father: Age: Yrs Religion and Caste: Original Native place if known: How common is consanguinity in the community: 2

ASSESMENT OF SYMPTOMATOLOGY I. FACIAL FEATURES: Coarse: Mild coarse: Normal: II. CNS FUNCTIONS: Mental Retardation: a. Severe MR b. Moderate MR c. Mild MR Regression of milestones Hypotonia Deep and superficial reflexes Power Myoclonal jerks Seizures Since how long Months/Yrs Cranial Nerves Signs of cord compression Hyperaccusis Hearing Status Aggressive Behavior Any Other [Please specify] 3

III. SKELETAL ABNORMALITIES: Dysostosis Multiplex Short Stature Bone crisis/osteonecrosis If present please specify the Signs. Status of joints and posture IV. SKIN/HAIR FINDINGS: Hypertrichosis Skin papules Telangiectasia Angiokeratomas Alopecia Any other (Please specify) V. EYE FINDINGS: Normal Cherry Red Spot Corneal Clouding Cataract Visual Blindness Any other (please specify) VI. CARDIOVASCULAR SYSTEM FINDINGS: ECG changes Cardiac failure Cardiomyopathy ECHO findings VII. HEPATOSPLENOMEGALY: 4

Hepatospleenomegaly Mild Moderate Severe VIII. HEMATOLOGICAL STUDY: Haemogram Blood/Bone marrow Vacuolated Lymphocytes Present/absent Specific Findings: ADDITIONAL INVESTIGATIONS: CT scan/mri: EEG: EMG/MCV: USG: X-Ray Others (BERA/ERG): SCORE: 0 Absent + Present ND= Not done NA= Not Available 5

Investigations: Screening test for common LSDs: Plasma/Serum Chitotriosidase (Screening for Gaucher and NPD) I-cell Screening (Screening for Mucolipidosis-II/III) Azure A test (MPS spot) (Screening for MPS) GAG Quantitative (Screening for MPS) GAG Qualitative (Screening for MPS) Enzyme Study (Lymphocytes and/or Plasma) Sr. No. Enzymes (Disease name) Proband Father Mother Mucopolysaccharidosis 1. -iduronidase (Hurler Syndrome, MPS-I) 2. α-iduronate Sulphate (from Plasma) (Hunter Syndrome, MPS-II) 3. Heparan Sulphamidase (Sanfilippo Syndrome type A, MPS IIIA) 4. N- acetyl- -glucosaminidase (from Plasma) (Sanfilippo Syndrome type B, MPS IIIB) 5. β-galactosidase-6-sulphate-sulphatase (Morquio Syndrome type A, MPS IVA) 6. β-galactosidase (Morquio Syndrome type B, MPS IVB) 7. Arylsulfatase B (Maroteaux- Lamy Syndrome, MPS VI) 8. -glucuronidase (Sly Syndrome, MPS VII) Defects in degradation of Glycolipids 9. -galactosidase (GM1 gangliosidosis) 6

10. Hexosaminidase-A (Tay-Sach s disease - GM2 gangliosidosis) 11. Hexosaminidase-T (Sandhoff disease - GM2 gangliosidosis) 12. -glucosidase (Gaucher disease) 13. Sphingomyelinase (Niemann Pick Disease A & B) 14. Acid Lipase (Wolman disease) Defects in degradation of sulphatides 15. Aryl A (Metachromatic Leucodystrophy, MLD) 16. -galactocerebrosidase (Krabbe disease) Defects in degradation of Glycogen 17. -1-4-glucosidase (Pompe disease, GSD II) With Acarbose: 18. Debrancher enzyme (GSD-III) Defects in degradation of Glycoproteins 19. -fucosidase (Fucosidosis) 20. - mannosidase (Mannosidosis) Defects in degradation of Globotriaosylceramide 21. α-galactosidase (Fabry disease) Defects in protein degradation (NCL) 22. Palmitoyl Protein Thioseterase (PPT) (Batten disease, NCL-I) 23. Tripeptidyl Peptidase-I (TPP-1) (Batten disease, NCL-II) Defects in lysosomal trafficking proteins 24. filipin stain (Cultured fibroblast) (Niemen-Pick disease C) Defects in lysosomal transporters Without Acarbose: 25 N-Acetyl-Neuraminic acid (NANA) (Urine) (Sialic acid storage disorders) Free NANA (Urine) Total NANA (Urine) Ratio: 7

Molecular Analysis: Table-1 Patients Name Variations previously reported for the phenotype in literature or databases and are recognized cause of clinical phenotype Gene Strand Genomic position cdna position (Ref. Sequence Number) Amino acid change Exon/ Intron no. Mutation status (Homozygous/ Heterozygous) Proband Mother Father Other (please specify) Table-2 Patients Name Variations previously unreported for the phenotype in literature or databases and are of the type that is expected to be the cause of the clinical phenotype Gene Strand Genomic position cdna position (Ref. Sequence Number) Amino acid change Exon/ Intron no. Mutation status (Homozygous/ Heterozygous) Proband Mother Father Other (please specify) 8

Table-3 Variations previously unreported for the phenotype and are of the type which may or may not be causative of the clinical phenotype Patients Name Gene Strand Genomic position cdna position (Ref. Sequence Number) Amino acid change Exon/ Intron no. Mutation status (Homozygous/ Heterozygous) Proband Mother Father Other (please specify) Insilico analysis: Location (Exon) Codon number Codon change Amino acid change Mutation T@ster score SIFT Score Polyphen2 Score (sensitivity, specificity) The Mutations T@ster score is taken from an amino acid substitution matrix (Grantham Matrix) which takes into account the physico-chemical characteristics of amino acids and scores substitutions according to the degree of difference between the original and the new amino acid scores may range from 0.0 to 6.0. The SIFT score is the normalized the probability that the amino acid change is tolerated and ranges from 0 to 1. The amino acid substitution is predicted damaging is the score id <=0.05, and tolerated if the score is >0.05. The Polyphen2 score is the naïve Bayes posterior to probability that this mutation is damaging and thus ranges from 0 to 1. 9

Clinical Photographs of Patient: Conclusion: 10

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