Author and year | Disease diagnosis | Demography (age, sex, consanguinity, ancestry/lineage, country of case reported) | Dermatoglyphic features |
---|---|---|---|
Goodman et al., 1972 [2] | Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases Clinically diagnosed | 17-years old Female (Proposita) No consanguinity Jewish Moroccan ancestry Reported from Israel | Digital dermatoglyphics: Whorls = 8 and extended beyond the borders of the terminal phalanges, TRC high = 271 Palmar dermatoglyphics: A–b ridge count = 73, ridge breath = 606, maximal atd angle = 110.5, modification of creases |
13-years old Male (affected brother) No consanguinity Jewish Moroccan ancestry Reported from Israel | Digital dermatoglyphics: Whorls=8 and extended beyond the borders of the terminal phalanges, TRC high = 350 Palmar dermatoglyphics: A–b ridge count=120, ridge breath=536, maximal atd angle=101.0, modification of crease | ||
Goodman et al., 1976 [1] | Tel Hashomer camptodactyly syndrome Clinically diagnosed | 20-years old Female (Proposita) Consanguineous parents Bedouin Reported from Israel | Digital dermatoglyphics: Whorls = 9, TRC high = 177 Palmar dermatoglyphics: A–b ridge count = 77, ridge breath = 493, maximal atd angle = 75, modification of crease |
19-years old Male (affected brother) Consanguineous parents Bedouin Reported from Israel | Digital dermatoglyphics: Whorls = 7, TRC high = 209 Palmar dermatoglyphics: A–b ridge count = 76, ridge breath = 697 maximal atd angle = 92, modification of crease | ||
Gollop and Colletto 1984 [9] | Tel Hashomer camptodactyly syndrome Clinically diagnosed Normal female chromosome | 7-years old Female (Proposita) Consanguineous parents Brazilian Reported from Brazil | Digital dermatoglyphics: Arches = 6, whorl = 2, ulnar loop = 2 TRC (LH = 11, RH = 14) Palmar dermatoglyphics: Bilateral transverse palmar crease, numerous additional palmar creases, vertical orientation of lines a and t, left hand the ulnarity index of patient 1 was decreased (0.51; mean Brazilian normal value 0.79 and 0.08, a–b RC (LH = 33, RH = 32), a–d RC (LH = 44, RH = 45), atd angle (LH = 40, RH = 35), main line index = (LH = 7, RH = 7) |
9-years old Male (affected brother) Consanguineous parents Brazilian Reported from Brazil | Digital dermatoglyphics: Arches=9 UL 1, TRC (LH = 0 RH = 1) Palmar dermatoglyphics: Bilateral transverse palmar creases, numerous white lines, and vertical orientation of lines a and t, the b triradius is absent and the atd angle is increased owing to a rare ulnar loop present in the hypothenar region at the level of the transverse palmar crease A–b RC = (LH = 0, RH = 42), a–b RC = (LH = 64, RH = 66), atd angle (LH = 107, RH = 106), main line index = (LH = 5, RH = 7) | ||
Tylki-Szymanska 1986 [10] | Tel Hashomer camptodactyly syndrome Clinically diagnosed | 13-years old Female (Proposita) Consanguineous parents (first cousins) Libyan family Reported from Poland | Abnormal hand prints + |
13-years old Male (Proposita) Consanguineous parents (first cousins) Libyan family Reported from Poland | Abnormal hand prints + | ||
10-years old Female (Proposita) Consanguineous parents (first cousins) Libyan family Reported from Poland | Abnormal hand prints + | ||
Patton et al., 1986 [11] | Tel Hashomer camptodactyly syndrome Clinically diagnosed | 4-years old Female (Proposita) No consanguinity Mother was English and father was Anglo-Asian origin Reported from UK | Palmar dermatoglyphics: Absent or decreased interphalangeal creases |
Pagnan et al., 1988 [12] | Tel Hashomer camptodactyly syndrome Clinically diagnosed Karyotype: chromosomes were normal (46,XX) | 4½-years old Female (Proposita) No consanguinity Ancestry : NR Reported from Brazil | Digital dermatoglyphics: Whorls 10/10, digital patterns are large, with displacement of triradii, TRC = 350 Palmar dermatoglyphics: A–b RC = 95, maximal atd 108.5, a–d count = 97, MLI = 16, modification of crease, simian crease of left hand, many “white lines” (shallow grooves of different length, width, and direction) on both palms and fingers and vertical orientation of the a, b, and t lines on the right and left hand |
Toriello et al., 1990 [7] | Tel Hashomer camptodactyly Clinically diagnosed | 15½-years old Male (Proposita) Consanguinity: NR Hispanic Reported from USA | Digital dermatoglyphics: Large whorls on each digit Palmar dermatoglyphics: A–d triradii, vertical a, b, and t lines, multiple white lines, and 2 palmar whorls on each hand |
11-years old Female (younger sister) Consanguinity: NR Hispanic Reported from USA | Digital dermatoglyphics: 9 large whorls and 1 ulnar loop Palmar dermatoglyphics: A triradius, vertical a, b, and t lines, and multiple white lines | ||
Franceschini et al., 1993 [13] | Tel Hashomer camptodactyly syndrome Clinically diagnosed | 17-years old Female (Proposita) Consanguineous parents (first cousins) Ancestry: NR Reported from Italy | Palmar dermatoglyphics: Bilateral transverse palmar creases, numerous additional palmar creases (so-called “white lines”), and ulnar displacement of t triradius |
Scarano et al. 1994 [18] | Tel Hashomer camptodactyly syndrome | Age: NRA Gender: NRA Consanguinity: NRA Ancestry: NRA Reported from Italy | Dermatoglyphics NRA |
Rogovina et al., 1995 [17] | Tel Hashomer camptodactyly syndrome | Patient 1 (siblings) Age, sex and ancestry NRA Consanguinity: NRA Reported from Russia | Flexion folds between phalanges were absent Other dermatoglyphic features NRA |
Patient 2 (siblings) Age, sex and ancestry NRA Consanguinity: NRA Reported from Russia | Flexion folds between phalanges were absent Other dermatoglyphic features NRA | ||
Patel and Adhia 2004 [14] | Tel Hashomer camptodactyly syndrome Clinically diagnosed Karyotype: 46,XX, chromosomal | 30-years old Female (Proposita) No consanguinity Ancestry: NR Reported from India | Abnormal dermatoglyphics + |
Age: NR Female (sister) No consanguinity Ancestry: NR Reported from India | Abnormal dermatoglyphics + | ||
Melegh et al., 2005 [15] | Tel Hashomer camptodactyly syndrome Clinically diagnosed Karyotype: normal | 4-years old Male (Proposita) No consanguinity Hungarian, followed up for 12 years Reported from Hungary | Digital dermatoglyphics: Whorl patterns on all ten fingertips, no other unusual ridges or flexion creases Palmar dermatoglyphics: No other unusual ridges or flexion creases were seen on the fingers, palms, and soles |
Smolkin et al., 2011 [5] | Tel Hashomer camptodactyly syndrome | Twin 1 monochorionic biamniotic 32-weeks 5-days old Male No consanguinity Ancestry: NR Reported from Israel | Digital dermatoglyphics: RH = absent interphalangeal crease in finger 5 LH = absent interphalangeal crease in finger 4, 5 Palmar dermatoglyphics: RH = simian crease LH = simian crease Partial absence of dermatoglyphic features |
Twin 1 monochorionic biamniotic 32-weeks 5-days old Male No consanguinity Ancestry: NR Reported from Israel | Digital dermatoglyphics: RH = absent interphalangeal crease in finger 2, 3, 4 LH = absent interphalangeal crease in finger 2, 3,4, 5 Palmar dermatoglyphics: RH = simian crease LH = simian crease Partial absence of dermatoglyphic features | ||
Shah et al., 2013 [16] | Tel Hashomer camptodactyly syndrome | 25-years old Male (Proposita) Consanguineous Ancestry: NR Reported from India | Dermatoglyphics not reported |