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Topic: .txt file to pdf with pdf page breaks inserted
Conf: (P-PDF) Developers, Msg: 51076
From: help
Date: 5/29/2002 04:42 PM
I have one .txt file consisting of 11000 records. They are each tagged with coding that indicates the beginning of each record. Is there a way that I can automatically convert to pdf with pdf page breaks between each record? I have included an example of one record from the .txt file below. I want to be able to make each record its own pdf file.
Thxs!
*RECORD*
*FIELD* NO
100050
*FIELD* TI
100050 AARSKOG SYNDROME
*FIELD* TX
Grier et al. (1983) reported father and 2 sons with typical Aarskog
syndrome, including short stature, hypertelorism, and shawl scrotum.
They tabulated the findings in 82 previous cases. X-linked recessive
inheritance has been repeatedly suggested (see 305400). The family
reported by Welch (1974) had affected males in 3 consecutive
generations. Thus, there is either genetic heterogeneity or this is an
autosomal dominant with strong sex-influence and possibly ascertainment
bias resulting from use of the shawl scrotum as a main criterion.
Stretchable skin was present in the cases of Grier et al. (1983). Teebi
et al. (1993) reported the case of an affected mother and 4 sons
(including a pair of monozygotic twins) by 2 different husbands. They
suggested that the manifestations were as severe in the mother as in the
sons and that this suggested autosomal dominant inheritance. Actually,
the mother seemed less severely affected, compatible with X-linked
inheritance.
*FIELD* RF
1. Grier, R. E.; Farrington, F. H.; Kendig, R.; Mamunes, P.: Autosomal
dominant inheritance of the Aarskog syndrome. Am. J. Med. Genet. 15:
39-46, 1983.
2. Teebi, A. S.; Rucquoi, J. K.; Meyn, M. S.: Aarskog syndrome: report
of a family with review and discussion of nosology. Am. J. Med. Genet. 46:
501-509, 1993.
3. Welch, J. P.: Elucidation of a 'new' pleiotropic connective tissue
disorder. Birth Defects Orig. Art. Ser. X(10): 138-146, 1974.
*FIELD* CS
Growth:
Mild to moderate short stature
Head:
Normocephaly
Hair:
Widow's peak
Facies:
Maxillary hypoplasia;
Broad nasal bridge;
Anteverted nostrils;
Long philtrum;
Broad upper lip;
Curved linear dimple below the lower lip
Eyes:
Hypertelorism;
Ptosis;
Down-slanted palpebral fissures;
Ophthalmoplegia;
Strabismus;
Hyperopic astigmatism;
Large cornea
Ears:
Floppy ears;
Lop-ears
Mouth:
Cleft lip/palate
GU:
Shawl scrotum;
Saddle-bag scrotum;
Cryptorchidism
Limbs:
Brachydactyly;
Digital contractures;
Clinodactyly;
Mild syndactyly;
Transverse palmar crease;
Lymphedema of the feet
Joints:
Ligamentous laxity;
Osteochondritis dissecans;
Proximal finger joint hyperextensibility;
Flexed distal finger joints;
Genu recurvatum;
Flat feet
Skin:
Stretchable skin
Spine:
Cervical spine hypermobility;
Odontoid anomaly
Heme:
Macrocytic anemia;
Hemochromatosis
GI:
Hepatomegaly;
Portal cirrhosis;
Imperforate anus;
Rectoperineal fistula
Pulmonary:
Interstitial pulmonary disease
Thorax:
Sternal deformity
Inheritance:
Sex-influenced autosomal dominant form;
also X-linked form
*FIELD* CD
Victor A. McKusick: 6/4/1986
*FIELD* ED
alopez: 06/03/1997
mimadm: 3/11/1994
carol: 7/7/1993
supermim: 3/16/1992
supermim: 3/20/1990
ddp: 10/26/1989
marie: 3/25/1988
